Version 4.0.200811





Short description of cell lines.
Species: human, Caucasian


- By selecting the cell line name, you will receive the detailed description of the cell line
- By selecting one of the terms between parentheses, you will receive the list of all rilevant cell line
- You can search any term of the list by using the 'Find' utility of your Browser

1301 (blood, leukemia, acute lymphoblastic T cell) - ICLC
162 (skin, fibroblast) - BGEBS
163 (skin, fibroblast) - BGEBS
2.2.15 (liver) - TOHEP
5637 (bladder, carcinoma) - ICLC
598_81H (fibroblast) - GGB
A-427 (lung, carcinoma) - DSMZ
A-427 (lung, carcinoma) - IZSBS
A-427 (lung, carcinoma) - MIEOS
A-549 (lung, carcinoma) - DSMZ
A-A94 (fibroblast, trisomy 21 / Down syndrome) - GGB
A-B92a (amnion) - GGB
A-B92f (fibroblast) - GGB
A-B92v (chorionic villi, chromosome mosaic) - GGB
A-C88 (amnion, trisomy 21 / Down syndrome) - GGB
A-P92 (amnion) - GGB
A-S91 (amnion, trisomy 21 / Down syndrome) - GGB
A09194 (fibroblast, chromosome aberration) - GGB
A1594 (fibroblast, chromosome aberration) - GGB
A2058 (skin, melanoma, metastatic) - ICLC
A549 (lung, carcinoma) - ECACC
A549 (lung, carcinoma) - GEUEM
A549 (lung, carcinoma) - ICLC
A549 (lung, carcinoma) - MIISB
A549 (lung, carcinoma) - MWIIW
A549 (lung, carcinoma) - SPBIC
A84M (lymphocyte) - GGB
A84P (lymphocyte) - GGB
A94 (fibroblast, camptomelic dwarfism) - GGB
A94M (lymphocyte) - GGB
A94P (lymphocyte) - GGB
A95 (fibroblast, dwarfism thanatophoric) - GGB
AA84F (fibroblast) - GGB
AAA95M (lymphocyte) - GGB
AC84 (lymphocyte, thanatophoric dwarfism) - GGB
AC95 (lymphocyte, cri du chat syndrome) - GGB
ACHN (kidney, adenocarcinoma) - ECACC
ACHN (kidney, adenocarcinoma) - ICLC
ACHN (kidney, adenocarcinoma) - IZSBS
AD94IL2 (lymphocyte) - GGB
AD94LEBV (lymphocyte) - GGB
AE84S (fibroblast) - GGB
AFA95M (lymphocyte) - GGB
AG 5025 (skin, fibroblast) - BGEBS
AG95P (lymphocyte) - GGB
AGLCL (lymphocyte, B) - ECACC
AGS (stomach, adenocarcinoma) - ECACC
AGS (stomach, adenocarcinoma) - IZSBS
AJ95 (lymphocyte, corpus callosum agenesis) - GGB
ALM86M (lymphocyte) - GGB
AM85 (lymphocyte) - GGB
AM86 (lymphocyte) - GGB
AM95 (lymphocyte, trisomy 21 / Down syndrome) - GGB
Amdur II (skin, fibroblast, methylmalonicacidemia) - ECACC
Amdur II (skin, fibroblast, methylmalonicacidemia) - IZSBS
AN86P (lymphocyte) - GGB
AP95 (lymphocyte, trisomy 21 / Down syndrome) - GGB
AR84S (lymphocyte) - GGB
AR91 (fibroblast, Fanconi anemia) - GGB
ARH 77 (peripheral blood, leukemia, plasma cell) - ECACC
AsPC-1 (pancreas, adenocarcinoma) - SPBIC
AT95 (lymphocyte, malformations) - GGB
B-A95 (amnion) - GGB
B-B87 (amnion) - GGB
B-B88a (amnion, trisomy 21 / Down syndrome) - GGB
B-B88f (fibroblast, trisomy 21 / Down syndrome) - GGB
B-B92c (umbilical cord) - GGB
B-B92s (skin) - GGB
B-C86 (amnion, trisomy 21 / Down syndrome) - GGB
B-C89 (amnion) - GGB
B-D93 (amnion, Down syndrome, mosaic) - GGB
B-F91 (amnion, Patau syndrome / trisomy 13) - GGB
B-G92 (amnion, Turner syndrome, mosaic) - GGB
B-K88 (amnion, trisomy 21 / Down syndrome) - GGB
B-L94 (amnion) - GGB
B-M 92a (amnion, trisomy 21 / Down syndrome) - GGB
B-M 92f (fibroblast, trisomy 21 / Down syndrome) - GGB
B-M91a (amnion, trisomy 21 / Down syndrome) - GGB
B-M91f (fibroblast, trisomy 21 / Down syndrome) - GGB
B-M93 (amnion) - GGB
B-P91 (amnion, Edwards' syndrome / trisomy 18) - GGB
B-P94 (amnion, trisomy 21 / Down syndrome) - GGB
B-R92 (amnion, chromosome aberration) - GGB
B-R93a (amnion, trisomy 21 / Down syndrome) - GGB
B-R93f (fibroblast, trisomy 21 / Down syndrome) - GGB
B-S95 (amnion, trisomy 21 / Down syndrome) - GGB
B-V92 (amnion) - GGB
B-Z94 (amnion, trisomy 21 / Down syndrome) - GGB
B192 (fibroblast, dyskeratosis) - GGB
B2195 (fibroblast, gastroschisis) - GGB
B84 (fibroblast) - GGB
B85 (fibroblast) - GGB
B86M (lymphocyte) - GGB
BA 93 (lymphocyte) - GGB
BA193 (lymphocyte) - GGB
BA96 (lymphocyte, trisomy 21 / Down syndrome) - GGB
BB96P (lymphocyte) - GGB
BC87IL2 (lymphocyte) - GGB
BC87ls (lymphocyte) - GGB
BC96 (fibroblast) - GGB
BE(2)-C (bone marrow, neuroblastoma) - ECACC
BE(2)-M17 (neural, neuroblastoma) - ECACC
BF93 (lymphocyte) - GGB
BF95 (lymphocyte) - GGB
BF96 (lymphocyte) - GGB
BG194 (lymphocyte) - GGB
BGF96M (lymphocyte) - GGB
BGP94 (lymphocyte) - GGB
BI96 (lymphocyte, tuberous sclerosis) - GGB
BL-41 (lymphoma, Burkitt) - DSMZ
BL-70 (lymphoma, Burkitt) - DSMZ
BL95 (lymphocyte, trisomy 21 / Down syndrome) - GGB
BLE96 (lymphocyte, tuberous sclerosis) - GGB
BLN96M (lymphocyte) - GGB
BM87 (lymphocyte) - GGB
BM95 (lymphocyte, trisomy 21 / Down syndrome) - GGB
BP86 (lymphocyte, chromosome aberration) - GGB
BP96 (lymphocyte, tuberous sclerosis) - GGB
BR96P (lymphocyte) - GGB
BT-20 (breast, carcinoma) - GEIAP
BT-20 (breast, carcinoma) - SPBIC
BT-20 (breast, carcinoma) - TOUCI
BT-474 (breast, carcinoma, ductal) - ICLC
BT-549 (breast, carcinoma, ductal) - ICLC
BT-B (cervix, carcinoma) - DSMZ
BUD-8 (skin, fibroblast) - ECACC
BUD-8 (skin, fibroblast) - IZSBS
C-4 II (cervix, carcinoma, cervical) - ECACC
C-4I (cervix, carcinoma, cervical) - ECACC
C-B94 (amnion, Edwards' syndrome / trisomy 18) - GGB
C-B95 (fibroblast, trisomy 21 / Down syndrome) - GGB
C-C87a (amnion, Edwards' syndrome / trisomy 18) - GGB
C-C87f (fibroblast, Edwards' syndrome / trisomy 18) - GGB
C-C90 (amnion, trisomy 21 / Down syndrome) - GGB
C-C91 (amnion, Klinefelter syndrome) - GGB
C-C95 (amnion, cri du chat syndrome) - GGB
C-D92 (amnion) - GGB
C-E 92 (amnion, trisomy 21 / Down syndrome) - GGB
C-F89 (fibroblast, trisomy 21 / Down syndrome) - GGB
C-G86 (amnion, trisomy 21 / Down syndrome) - GGB
C-M87 (fibroblast) - GGB
C-M92 (fibroblast, trisomy 21 / Down syndrome) - GGB
C-N90 (amnion, trisomy 21 / Down syndrome) - GGB
C-N95 (fibroblast, trisomy 21 / Down syndrome) - GGB
C-S91a (amnion, trisomy 21 / Down syndrome) - GGB
C-S95 (amnion, chromosome aberration) - GGB
C0092 (amnion, D. Becker syndrome) - GGB
C0994IL2 (lymphocyte, chromosome aberration) - GGB
C1191f (fibroblast, trisomy 14) - GGB
C1191v (fibroblast, trisomy 14) - GGB
C1192 (fibroblast, trisomy 7) - GGB
C1195 (fibroblast, Edwards' syndrome / trisomy 18) - GGB
C1293 (fibroblast, trisomy 21 / Down syndrome) - GGB
C1294a (amnion) - GGB
C1294f (fibroblast) - GGB
C1595a (amnion) - GGB
C1595f (fibroblast) - GGB
C1PV (skin, fibroblast) - PVCGU
C211 (skin, cri du chat syndrome) - ECACC
C2PV (skin, fibroblast) - PVCGU
C33A (cervix, carcinoma) - ICLC
C3PV (skin, fibroblast) - PVCGU
C4PV (skin, fibroblast) - PVCGU
C5PV (skin, fibroblast) - PVCGU
C6PV (skin, fibroblast, porokeratosis of Mibelli) - PVCGU
C7PV (skin, fibroblast, photosensitivity) - PVCGU
C83 (fibroblast) - GGB
C86M (lymphocyte) - GGB
C86P (lymphocyte) - GGB
C87 (fibroblast) - GGB
C8PV (skin, fibroblast) - PVCGU
C91 (fibroblast, chromosome mosaic) - GGB
C92 (fibroblast, D. Becker syndrome) - GGB
C93 (fibroblast, Pallister Killian syndrome) - GGB
C96 (amnion, trisomy 21 / Down syndrome) - GGB
C9PV (skin, fibroblast) - PVCGU
Ca Ski (cervix, carcinoma, epidermoid) - ECACC
Ca Ski (cervix, carcinoma) - MIISA
Ca Ski (cervix, carcinoma) - MIISB
CA295 (lymphocyte) - GGB
CA95 (lymphocyte, trisomy 21 / Down syndrome) - GGB
CA96 (lymphocyte, familial epylepsy) - GGB
CACO-2 (colon, adenocarcinoma) - DSMZ
CACO-2 (colon, adenocarcinoma) - ECACC
Caco-2 (colon, adenocarcinoma) - ICLC
Caco-2 (colon, adenocarcinoma) - IZSBS
Caco-2 (colon, adenocarcinoma) - MIECC
Caco-2 (colon, adenocarcinoma) - MIUFC
Caco-2 (colon, adenocarcinoma) - RMSTC
Caco-2 (colon, adenocarcinoma) - SPBIC
CAKI 2 (kidney, carcinoma) - ECACC
Caki-1 (kidney, carcinoma) - IZSBS
Caki-2 (kidney, carcinoma) - ICLC
Caki-2 (kidney, carcinoma) - IZSBS
CALU 1 (lung, carcinoma, epidermoid) - ECACC
Calu-1 (lung, carcinoma, epidermoid, grade III) - ICLC
CaLu-1 (lung, carcinoma, epidermoid) - IZSBS
Calu-3 (lung, adenocarcinoma) - GEUEM
Calu-3 (lung, adenocarcinoma) - IZSBS
Calu-3 (lung, adenocarcinoma) - MIISB
Calu-6 (lung, adenocarcinoma) - GEUEM
Calu-6 (lung, carcinoma, anaplastic) - ICLC
CAPAN 1 (pancreas, adenocarcinoma) - IZSBS
CAPAN 2 (pancreas, carcinoma) - IZSBS
CAPAN-1 (pancreas, adenocarcinoma) - DSMZ
CAPAN-2 (pancreas, adenocarcinoma) - DSMZ
Capan-2 (pancreas, adenocarcinoma) - SPBIC
CaSki (cervix, carcinoma, epidermoid, from metastatic site) - ICLC
CC96 (lymphocyte, neurofibromatosis type I) - GGB
CCD 16Lu (lung) - ECACC
CCD 19Lu (lung) - ECACC
CCD 25Lu (lung) - ECACC
CCD 8Lu (lung) - ECACC
CCD-32Lu (lung) - ECACC
CCD-33Lu (lung) - ECACC
CCD-37Lu (lung) - ECACC
CCD-39Lu (lung) - ECACC
CCF-STTG1 (brain, astrocytoma) - ECACC
CCF-STTG1 (astrocytoma, anaplastic, grade IV) - IZSBS
CCM89M (lymphocyte) - GGB
CCRF-CEM (peripheral blood, leukemia, acute lymphoblastic) - ECACC
CCRF-CEM (peripheral blood, leukemia, acute lymphoblastic) - IZSBS
CCRF-CEM (peripheral blood, leukemia, acute lymphoblastic) - PSHTM
CCRF-HSB-2 (peripheral blood, leukemia, acute lymphoblastic T cell) - ECACC
CCRF-SB (peripheral blood, leukemia, acute lymphoblastic) - ECACC
CCRF-SB (peripheral blood, leukemia, acute lymphoblastic) - IZSBS
CCRF-SB (peripheral blood, leukemia, acute lymphoblastic) - SPBIC
CD88f (fibroblast, Down syndrome, mosaic) - GGB
CD88ls (lymphocyte, Down syndrome, mosaic) - GGB
CD89P (fibroblast) - GGB
CDM96 (lymphocyte, familial epylepsy) - GGB
CF84f (fibroblast, Down syndrome, mosaic) - GGB
CF84ls (lymphocyte, Down syndrome, mosaic) - GGB
CF89P (lymphocyte) - GGB
CF96F (lymphocyte) - GGB
CF96P (lymphocyte) - GGB
CFPAC-1 (pancreas, adenocarcinoma) - ECACC
CFPAC-1 (pancreas, adenocarcinoma, ductal) - ICLC
CG89 (lymphocyte, chromosome aberration) - GGB
CG94IL2 (lymphocyte, chromosome aberration) - GGB
CG96 (lymphocyte, neurofibromatosis type I) - GGB
Citrullinemia (skin, citrullinemia) - ECACC
CL95 (lymphocyte, trisomy 21 / Down syndrome) - GGB
CL96f (fibroblast, erythroblastopenia, transient) - GGB
CL96IL2 (lymphocyte, familial epylepsy) - GGB
CLM96M (lymphocyte) - GGB
Clone 15 HL-60 (leukemia, promyelocytic) - ECACC
CM-S/un (bone marrow, monocyte tumor) - ICLC
CM87 (lymphocyte, trisomy 21 / Down syndrome) - GGB
CM87IL2 (lymphocyte, trisomy 21 / Down syndrome) - GGB
CM88M (lymphocyte) - GGB
CM91IL2 (lymphocyte, chromosome aberration) - GGB
CM91ls (lymphocyte, Turner syndrome/noonan syndrome 1) - GGB
CM94 (lymphocyte) - GGB
CM94P (lymphocyte) - GGB
CMR94M (lymphocyte) - GGB
CN96 (lymphocyte) - GGB
COLO 201 (colon, adenocarcinoma) - ECACC
COLO 205 (colon, adenocarcinoma) - ECACC
COLO 205 (colon, colorectal adenocarcinoma) - ICLC
COLO 320DM (colon, adenocarcinoma) - ECACC
COLO 320HSR (colon, adenocarcinoma) - ECACC
COLO 320HSR (colon, adenocarcinoma) - SPBIC
COLO 839 (lymphocyte, B, melanoma) - ECACC
COLO-320 (colon, adenocarcinoma) - DSMZ
COLO-849 (melanoma, metastatic) - DSMZ
Cor Per (skin, fibroblast, Ehlers-Danlos syndrome, type IV, autosomal dominant) - BGEBS
COR-L105 (lung, adenocarcinoma) - ECACC
COR-L23 (lung, carcinoma, large cell) - ECACC
COR-L23 (lung, carcinoma, large cell) - ICLC
COR-L47 (bone marrow, carcinoma, lung small cell) - ECACC
COR-L51 (lung, carcinoma, lung small cell) - ECACC
COR-L88 (pleural effusion, carcinoma, lung small cell) - ECACC
CR83 (fibroblast, epidermolysis bullo'sa) - GGB
CR88P (lymphocyte) - GGB
CR96 (lymphocyte, epilepsy) - GGB
Cri du Chat (skin, fibroblast, cri du chat syndrome) - ECACC
CS191 (fibroblast, Turner syndrome, mosaic) - GGB
CS1PV (skin, fibroblast, Cockayne syndrome) - PVCGU
CS87 (lymphocyte, T, trisomy 21 / Down syndrome) - GGB
CS96 (fibroblast, Freeman-Sheldon syndrome) - GGB
CT96 (lymphocyte, hypercholesterolemia, familial) - GGB
CV96F (lymphocyte) - GGB
CVD89M (lymphocyte) - GGB
D-A92a (amnion, trisomy 21 / Down syndrome) - GGB
D-A92f (fibroblast, trisomy 21 / Down syndrome) - GGB
D-B87 (amnion) - GGB
D-C95 (amnion) - GGB
D-F92 (fibroblast, trisomy 21 / Down syndrome) - GGB
D-F94 (amnion, trisomy 21 / Down syndrome) - GGB
D-G92 (fibroblast, trisomy 21 / Down syndrome) - GGB
D-M89 (amnion, Patau syndrome / trisomy 13) - GGB
D-R86 (amnion, Edwards' syndrome / trisomy 18) - GGB
D-T93 (amnion) - GGB
D0994 (fibroblast) - GGB
D1589 (fibroblast) - GGB
D2085 (fibroblast) - GGB
D2187 (fibroblast, anencephaly) - GGB
D94 (fibroblast, Miller-Dieker syndrome) - GGB
D96 (fibroblast) - GGB
Da Mo (skin, fibroblast, Ehlers-Danlos syndrome, type V) - BGEBS
DA94 (fibroblast, Patau syndrome / trisomy 13) - GGB
DB-R95 (amnion) - GGB
DBC95 (lymphocyte, trisomy 21 / Down syndrome) - GGB
DBM96 (lymphocyte, neurofibromatosis type I) - GGB
DBV95 (lymphocyte, trisomy 21 / Down syndrome) - GGB
DC-P87 (amnion, trisomy 21 / Down syndrome) - GGB
DC96 (lymphocyte, familial epylepsy) - GGB
DCi96 (lymphocyte, familial epylepsy) - GGB
DCo96 (lymphocyte, familial epylepsy) - GGB
DCon96 (lymphocyte, familial epylepsy) - GGB
DDC95 (lymphocyte, T, trisomy 21 / Down syndrome) - GGB
DE96P (lymphocyte) - GGB
Detroit 510 (skin, fibroblast, galactosemia) - ECACC
Detroit 510 (skin, fibroblast, galactosemia) - IZSBS
Detroit 525 (skin, fibroblast, Turner syndrome/noonan syndrome 1) - ECACC
Detroit 525 (skin, fibroblast, Turner syndrome/noonan syndrome 1) - IZSBS
Detroit 529 (skin, fibroblast, trisomy 21 / Down syndrome) - ECACC
Detroit 529 (skin, fibroblast, trisomy 21 / Down syndrome) - IZSBS
Detroit 532 (skin, trisomy 21 / Down syndrome) - ECACC
Detroit 532 (foreskin, trisomy 21 / Down syndrome) - IZSBS
Detroit 539 (skin, fibroblast, trisomy 21 / Down syndrome) - ECACC
Detroit 539 (skin, fibroblast, trisomy 21 / Down syndrome) - IZSBS
Detroit 548 (skin, fibroblast, partial D trisomy) - IZSBS
Detroit 551 (skin, embryonic) - ECACC
Detroit 551 (skin, embryonic) - IZSBS
Detroit 562 (pharynx, carcinoma) - ECACC
Detroit 562 (pharynx, carcinoma) - IZSBS
Detroit 573 (skin, fibroblast, B/D translocation) - ECACC
Detroit 573 (skin, fibroblast, B/D translocation) - IZSBS
DFA96M (lymphocyte) - GGB
DFC96 (lymphocyte, familial epylepsy) - GGB
DFF87 (lymphocyte, trisomy 21 / Down syndrome) - GGB
DFGe96 (lymphocyte, familial epylepsy) - GGB
DFGi96 (lymphocyte, familial epylepsy) - GGB
DG96 (lymphocyte, familial epylepsy) - GGB
DL86 (fibroblast, severe combined immunodeficiency disease) - GGB
DL87 (fibroblast) - GGB
DLF87 (fibroblast) - GGB
DLG96f (fibroblast, Down syndrome, mosaic) - GGB
DLG96IL2 (lymphocyte, Down syndrome, mosaic) - GGB
DLL87S (fibroblast) - GGB
DM94 (lymphocyte, Angelman syndrome) - GGB
DMM87 (lymphocyte) - GGB
DMS 153 (lung, carcinoma, small cell) - ECACC
DMS 454 (lung, carcinoma, small cell) - ECACC
DMS 53 (lung, carcinoma, small cell) - ECACC
DMS 92 (lung, carcinoma, small cell) - ECACC
DOK (tongue, carcinoma) - ECACC
DP-LL95 (amnion, trisomy 21 / Down syndrome) - GGB
DPS84 (fibroblast, osteogenesis imperfecta) - GGB
DR89P (lymphocyte) - GGB
DS 92 (fibroblast, trisomy 21 / Down syndrome) - GGB
DSH1PV (skin, fibroblast, dyschromatosis symmetrica hereditaria) - PVCGU
DSH2PV (skin, fibroblast, dyschromatosis symmetrica hereditaria) - PVCGU
DSH3PV (skin, fibroblast, dyschromatosis symmetrica hereditaria) - PVCGU
DSH4PV (skin, fibroblast, dyschromatosis symmetrica hereditaria) - PVCGU
DU 145 (prostate, carcinoma) - IZSBS
DU 145 (prostate, carcinoma) - MIUEP
DU-145 (prostate, carcinoma) - ICLC
DVA96 (lymphocyte, familial epylepsy) - GGB
E-P95 (amnion, Meckel syndrome) - GGB
E.H.IV (Elaine IV) (blood, infectious mononucleosis) - ECACC
EDS 100 (skin, fibroblast, Ehlers-Danlos syndrome, type III) - BGEBS
EDS 101 (skin, fibroblast, Ehlers-Danlos syndrome, type III) - BGEBS
EDS 105 (skin, fibroblast, Ehlers-Danlos syndrome, type VII) - BGEBS
EFE-184 (endometrium, carcinoma) - DSMZ
EFM-19 (breast, carcinoma) - DSMZ
EFO-21 (ovary, cystoadenocarcinoma) - DSMZ
EM-2 (bone marrow, leukemia, chronic myeloid) - DSMZ
EM-3 (bone marrow, leukemia, chronic myeloid) - DSMZ
Eos-HL-60 (blood, leukemia, promyelocytic) - ECACC
ES-095 (amnion) - GGB
F-C87 (amnion) - GGB
F-D96 (amnion) - GGB
F-M91 (amnion) - GGB
F-M96 (amnion) - GGB
F-P89 (amnion) - GGB
F-P95 (fibroblast, trisomy 21 / Down syndrome) - GGB
F-P96 (amnion, anencephaly) - GGB
F0091 (fibroblast, trisomy 5) - GGB
F0894 (fibroblast) - GGB
F1187 (fibroblast, trisomy 16) - GGB
F1293 (fibroblast, trisomy 21 / Down syndrome) - GGB
F1792 (fibroblast, hydrocephalus) - GGB
F2586 (fibroblast) - GGB
F7000 (foreskin) - BGEBS
F89 (fibroblast, trisomy 21 / Down syndrome) - GGB
F94 (fibroblast, camptomelic dwarfism) - GGB
F95 (fibroblast, Martin-Bell syndrome) - GGB
F96 (fibroblast, Marfan syndrome) - GGB
FC96IL2 (lymphocyte) - GGB
FC96ls (lymphocyte) - GGB
FE92 (lymphocyte) - GGB
Fer Ray (skin, fibroblast, Ehlers-Danlos syndrome, type VIII) - BGEBS
FFC87M (lymphocyte) - GGB
FG186 (fibroblast) - GGB
FG86 (lymphocyte, trisomy 21 / Down syndrome) - GGB
FGC95 (lymphocyte, trisomy 21 / Down syndrome) - GGB
FGF96 (lymphocyte, neurofibromatosis type I) - GGB
FH 1 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 10 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 100 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 101 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 103 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 105 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 106 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 111 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 112 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 113 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 114 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 118 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 119 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 120 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 121 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 124 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 125 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 126 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 129 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 13 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 130 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 131 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 132 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 133 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 134 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 135 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 136 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 137 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 138 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 14 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 140 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 141 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 142 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 143 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 144 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 145 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 146 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 147 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 148 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 149 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 15 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 150 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 151 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 152 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 153 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 154 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 155 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 156 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 157 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 16 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 160 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 161 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 162 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 163 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 164 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 165 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 167 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 168 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 169 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 17 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 170 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 171 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 172 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 176 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 177 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 178 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 18 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 19 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 20 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 21 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 22 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 23 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 24 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 25 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 26 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 27 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 29 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 30 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 31 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 32 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 33 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 34 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 35 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 36 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 37 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 38 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 39 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 4 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 47 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 49 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 5 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 50 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 51 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 52 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 53 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 54 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 55 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 56 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 57 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 59 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 6 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 60 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 61 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 62 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 63 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 64 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 65 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 66 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 67 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 68 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 69 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 7 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 70 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 71 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 72 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 73 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 74 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 75 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 76 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 77 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 78 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 79 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 8 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 80 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 81 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 82 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 83 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 84 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 85 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 86 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 9 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 91 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 92 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 93 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 94 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 95 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 96 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 97 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 98 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FH 99 (skin, fibroblast, hypercholesterolemia, familial) - DSB
FIB-CL1 (skin, fibroblast, cutis laxa, recessive, type I) - DSB
FIB-CL10 (skin, fibroblast, cutis laxa, recessive, type I) - DSB
FIB-CL2 (skin, fibroblast, cutis laxa, recessive, type I) - DSB
FIB-CL3 (skin, fibroblast, cutis laxa, recessive, type I) - DSB
FIB-CL5 (skin, fibroblast, cutis laxa, recessive, type I) - DSB
FIB-CL6 (skin, fibroblast, cutis laxa, recessive, type I) - DSB
FIB-CL7 (skin, fibroblast, cutis laxa, recessive, type I) - DSB
FIB-CL8 (skin, fibroblast, cutis laxa, recessive, type I) - DSB
FIB-CL9 (skin, fibroblast, cutis laxa, recessive, type I) - DSB
FIB-DUP1 (skin, fibroblast, Dupuytren contracture) - DSB
FIB-DUP10 (skin, fibroblast, Dupuytren contracture) - DSB
FIB-DUP11 (skin, fibroblast, Dupuytren contracture) - DSB
FIB-DUP14 (skin, fibroblast, Dupuytren contracture) - DSB
FIB-DUP15 (skin, fibroblast, Dupuytren contracture) - DSB
FIB-DUP3 (skin, fibroblast, Dupuytren contracture) - DSB
FIB-DUP4 (skin, fibroblast, Dupuytren contracture) - DSB
FIB-DUP5 (skin, fibroblast, Dupuytren contracture) - DSB
FIB-DUP6 (skin, fibroblast, Dupuytren contracture) - DSB
FIB-DUP7 (skin, fibroblast, Dupuytren contracture) - DSB
FIB-DUP9 (skin, fibroblast, Dupuytren contracture) - DSB
FIB-EDII1 (skin, fibroblast, Ehlers-Danlos syndrome) - DSB
FIB-EDII11 (skin, fibroblast, Ehlers-Danlos syndrome) - DSB
FIB-EDIII5 (skin, fibroblast, Ehlers-Danlos syndrome) - DSB
FIB-EDIV2 (skin, fibroblast, Ehlers-Danlos syndrome) - DSB
FIB-EDIV4 (skin, fibroblast, Ehlers-Danlos syndrome) - DSB
FIB-IP1 (skin, fibroblast, cutaneous hyperlaxity) - DSB
FIB-IP2 (skin, fibroblast, cutaneous hyperlaxity) - DSB
FIB-LARSEN1 (skin, fibroblast, Larsen syndrome) - DSB
FIB-LARSEN2 (skin, fibroblast, Larsen syndrome) - DSB
FIB-MARFAN1 (skin, fibroblast, Marfan syndrome) - DSB
FIB-MARFAN3 (skin, fibroblast, Marfan syndrome) - DSB
FIB-MARFAN4 (skin, fibroblast, Marfan syndrome) - DSB
FIB-MARFAN5 (skin, fibroblast, Marfan syndrome) - DSB
FIB-MARFAN6 (skin, fibroblast, Marfan syndrome) - DSB
FIB-MOR1 (skin, fibroblast, mucopolysaccharidosis type IV B / Morquio syndrome) - DSB
FIB-NC15 (skin, fibroblast) - DSB
FIB-NC16 (skin, fibroblast) - DSB
FIB-NC23 (skin, fibroblast) - DSB
FIB-NC25 (skin, fibroblast) - DSB
FIB-NC27 (skin, fibroblast) - DSB
FIB-NC30 (skin, fibroblast) - DSB
FIB-NC42 (skin, fibroblast) - DSB
FIB-NC46 (skin, fibroblast) - DSB
FIB-NC54 (skin, fibroblast) - DSB
FIB-NC55 (skin, fibroblast) - DSB
FIB-NC56 (skin, fibroblast) - DSB
FIB-NC57 (skin, fibroblast) - DSB
FIB-NC58 (skin, fibroblast) - DSB
FIB-NC59 (skin, fibroblast) - DSB
FIB-NC60 (skin, fibroblast) - DSB
FIB-NC62 (skin, fibroblast) - DSB
FIB-NC63 (skin, fibroblast) - DSB
FIB-NC64 (skin, fibroblast) - DSB
FIB-NC65 (skin, fibroblast) - DSB
FIB-NC66 (skin, fibroblast) - DSB
FIB-NC67 (skin, fibroblast) - DSB
FIB-PROL1 (skin, fibroblast, prolidase deficiency) - DSB
FIB-PROL2 (skin, fibroblast, prolidase deficiency) - DSB
FIB-PSE1 (skin, fibroblast, pseudoxanthoma elasticum) - DSB
FIB-PSE12 (skin, fibroblast, pseudoxanthoma elasticum) - DSB
FIB-PSE13 (skin, fibroblast, pseudoxanthoma elasticum) - DSB
FIB-PSE14 (skin, fibroblast, pseudoxanthoma elasticum) - DSB
FIB-PSE15 (skin, fibroblast, pseudoxanthoma elasticum) - DSB
FIB-PSE17 (skin, fibroblast, pseudoxanthoma elasticum) - DSB
FIB-PSE2 (skin, fibroblast, pseudoxanthoma elasticum) - DSB
FIB-PSE26 (skin, fibroblast, pseudoxanthoma elasticum) - DSB
FIB-PSE3 (skin, fibroblast, pseudoxanthoma elasticum) - DSB
FIB-PSE32 (skin, fibroblast, pseudoxanthoma elasticum) - DSB
FIB-PSE34 (skin, fibroblast, pseudoxanthoma elasticum) - DSB
FIB-PSE35 (skin, fibroblast, pseudoxanthoma elasticum) - DSB
FIB-PSE39 (skin, fibroblast, pseudoxanthoma elasticum) - DSB
FIB-PSE40 (skin, fibroblast, pseudoxanthoma elasticum) - DSB
FIB-PSE43 (skin, fibroblast, pseudoxanthoma elasticum) - DSB
FIB-PSE44 (skin, fibroblast, pseudoxanthoma elasticum) - DSB
FIB-PSE45 (skin, fibroblast, pseudoxanthoma elasticum) - DSB
FIB-PSE46 (skin, fibroblast, pseudoxanthoma elasticum) - DSB
FIB-PSE47 (skin, fibroblast, pseudoxanthoma elasticum) - DSB
FIB-PSE50 (skin, fibroblast, pseudoxanthoma elasticum) - DSB
FIB-PSE51 (skin, fibroblast, pseudoxanthoma elasticum) - DSB
FIB-PSE52 (skin, fibroblast, pseudoxanthoma elasticum) - DSB
FIB-PSE53 (skin, fibroblast, pseudoxanthoma elasticum) - DSB
FIB-PSE54 (skin, fibroblast, pseudoxanthoma elasticum) - DSB
FIB-SCLE1 (skin, fibroblast, scleroderma, familial progressive) - DSB
FIB-SCLE10 (skin, fibroblast, scleroderma, familial progressive) - DSB
FIB-SCLE11 (skin, fibroblast, scleroderma, familial progressive) - DSB
FIB-SCLE12 (skin, fibroblast, scleroderma, familial progressive) - DSB
FIB-SCLE13 (skin, fibroblast, scleroderma, familial progressive) - DSB
FIB-SCLE14 (skin, fibroblast, scleroderma, familial progressive) - DSB
FIB-SCLE15 (skin, fibroblast, scleroderma, familial progressive) - DSB
FIB-SCLE16 (skin, fibroblast, scleroderma, familial progressive) - DSB
FIB-SCLE17 (skin, fibroblast, scleroderma, familial progressive) - DSB
FIB-SCLE18 (skin, fibroblast, scleroderma, familial progressive) - DSB
FIB-SCLE19 (skin, fibroblast, scleroderma, familial progressive) - DSB
FIB-SCLE2 (skin, fibroblast, scleroderma, familial progressive) - DSB
FIB-SCLE20 (skin, fibroblast, scleroderma, familial progressive) - DSB
FIB-SCLE21 (skin, fibroblast, scleroderma, familial progressive) - DSB
FIB-SCLE3 (skin, fibroblast, scleroderma, familial progressive) - DSB
FIB-SCLE4 (skin, fibroblast, scleroderma, familial progressive) - DSB
FIB-SCLE5 (skin, fibroblast, scleroderma, familial progressive) - DSB
FIB-SCLE6 (skin, fibroblast, scleroderma, familial progressive) - DSB
FIB-SCLE7 (skin, fibroblast, scleroderma, familial progressive) - DSB
FIB-SCLE8 (skin, fibroblast, scleroderma, familial progressive) - DSB
FIB-SCLE9 (skin, fibroblast, scleroderma, familial progressive) - DSB
FL88 (lymphocyte) - GGB
FMG87 (lymphocyte) - GGB
FN86 (lymphocyte, trisomy 21 / Down syndrome) - GGB
FV93 (fibroblast, Turner syndrome/noonan syndrome 1) - GGB
G-292 Clone A141B1 (bone, osteosarcoma) - ECACC
G-361 (skin, malignant melanoma) - BGEBS
G-361 (skin, malignant melanoma) - ECACC
G-401 (kidney) - ECACC
G-402 (kidney, leiomyoblastoma) - ECACC
G-A88 (amnion, trisomy 21 / Down syndrome) - GGB
G-B90 (amnion) - GGB
G-C195 (amnion, Edwards' syndrome / trisomy 18) - GGB
G-C92 (amnion, trisomy 21 / Down syndrome) - GGB
G-C94 (fibroblast, trisomy 21 / Down syndrome) - GGB
G-C95 (amnion, anencephaly) - GGB
G-F92a (amnion, trisomy 21 / Down syndrome) - GGB
G-F92f (fibroblast, trisomy 21 / Down syndrome) - GGB
G-F95 (amnion) - GGB
G-L88 (fibroblast, trisomy 21 / Down syndrome) - GGB
G-M89 (amnion, Edwards' syndrome / trisomy 18) - GGB
G-M95a (amnion, trisomy 21 / Down syndrome) - GGB
G-M95f (fibroblast, trisomy 21 / Down syndrome) - GGB
G0086 (fibroblast, trisomy 16) - GGB
G0895 (fibroblast, Patau syndrome / trisomy 13) - GGB
G1094 (fibroblast) - GGB
G1291 (fibroblast, trisomy 7) - GGB
G25496 (lymphocyte, hypercholesterolemia, familial) - GGB
GA87 (skin, fibroblast, trisomy 21 / Down syndrome) - GGB
GA93 (lymphocyte) - GGB
GA96 (lymphocyte, neurofibromatosis type I) - GGB
GAa85F (lymphocyte) - GGB
GAi85F (lymphocyte) - GGB
GB95 (lymphocyte, hypercholesterolemia, familial) - GGB
GC95 (lymphocyte, hypercholesterolemia, familial) - GGB
GE86 (lymphocyte, trisomy 21 / Down syndrome) - GGB
GE95 (lymphocyte, trisomy 21 / Down syndrome) - GGB
GG87 (lymphocyte) - GGB
GGP87F (lymphocyte) - GGB
GI-CA-N (neuroblastoma) - GEIOP
GI-CA-N (neuroblastoma) - ICLC
GI-LI-N (neuroblastoma) - GEIOP
GI-LI-N (neuroblastoma) - ICLC
GI-ME-N (neuroblastoma) - GEIOP
GI-ME-N (bone marrow, metastatic neuroblastoma, stage IV) - ICLC
GI95 (lymphocyte, hypercholesterolemia, familial) - GGB
GM 490 (lymphoma) - PSHIM
GM00112A (fibroblast, Niemann-Pick disease, type A) - MIECC
GM00135A (fibroblast, hypercholesterolemia, familial) - MIECC
GM00469 (fibroblast, adenosine deaminase) - MIECC
GM00483 (fibroblast, hypercholesterolemia, familial) - MIECC
GM00488C (fibroblast, hypercholesterolemia, familial) - MIECC
GM00637B (skin, fibroblast) - NAUBC
GM00863 (fibroblast, Wolman disease/cholesterol ester storage disease) - MIECC
GM00881 (fibroblast, angiokeratoma, diffuse / Fabry disease) - MIECC
GM01607 (fibroblast, Gaucher disease type I) - MIECC
GM02185 (skin, fibroblast) - GEIMG
GM02290 (skin, fibroblast, Lesch-Nyhan syndrome) - MIISA
GM02291 (lung, embryonic, Lesch-Nyhan syndrome) - MIISA
GM02605 (fibroblast) - GEIMG
GM02824 (fibroblast) - GEIMG
GM02848 (skin, fibroblast) - BGEBS
GM03123 (fibroblast, Niemann-Pick disease) - MIECC
GM03252 (fibroblast, Niemann-Pick disease, type B) - MIECC
GM05752 (fibroblast, Farber lipogranulomatosis) - MIECC
GM05870 (fibroblast, acyl-CoA dehydrogenase, medium-chain, deficiency) - MIECC
GM06127 (fibroblast, acyl-CoA dehydrogenase, long-chain, deficiency) - MIECC
GM08866 (fibroblast, acyl-CoA dehydrogenase, short-chain, deficiency) - MIECC
GM87 (lymphocyte) - GGB
GM95 (lymphocyte, trisomy 21 / Down syndrome) - GGB
GP2d (colon, adenocarcinoma) - ECACC
GP5d (colon, adenocarcinoma) - ECACC
GR-M (skin, melanoma) - ECACC
GR95 (lymphocyte, trisomy 21 / Down syndrome) - GGB
GS-109-V-20 (skin, fibroblast, Gardner's syndrome) - ECACC
GS-109-V-34 (skin, fibroblast, Gardner's syndrome) - ECACC
GS-109-V-63 (skin, fibroblast, Gardner's syndrome) - ECACC
GS83f (fibroblast, Down syndrome, mosaic) - GGB
GS83ls (lymphocyte, Down syndrome, mosaic) - GGB
GS93 (fibroblast, Fanconi anemia) - GGB
GT186f (fibroblast, hermaphroditism true) - GGB
GT186ls (lymphocyte, hermaphroditism true) - GGB
GT86f (fibroblast, hermaphroditism true) - GGB
GT86ls (lymphocyte) - GGB
H-A88 (amnion, trisomy 21 / Down syndrome) - GGB
H4 (brain, nervous tissue glial tumor) - IZSBS
H9 (lymphocyte, T, lymphoma) - ICLC
HBL-100 (breast, cancer) - SPBIC
HECV (umbilical cord) - ICLC
HEL (skin, fibroblast) - GEIMM
HEL 299 (lung, embryonic) - BGEBS
HEL 299 (lung, embryonic) - IZSBS
HEL 299 (lung, embryonic) - PNIOS
HEL 92.1.7 (blood, erythroleukemia) - ECACC
HEL 92.1.7 (erythroleukemia) - ICLC
Hep 2 (larynx, carcinoma, epidermoid) - IZSBS
Hep G2 (liver, carcinoma, hepatocellular) - ECACC
Hep G2 (liver, carcinoma, hepatocellular) - GEUCC
Hep G2 (liver, carcinoma, hepatocellular) - ICLC
Hep G2 (liver, carcinoma, hepatocellular) - IZSBS
Hep G2 (liver, carcinoma, hepatocellular) - MIECC
Hep G2 (liver, carcinoma, hepatocellular) - MIUFC
Hep G2 (liver, carcinoma, hepatocellular) - PGUPG
Hep G2 (liver, carcinoma, hepatocellular) - SPBIC
Hep G2 (liver, carcinoma, hepatocellular) - TOHEP
HEp-2 (larynx, carcinoma, squamous cell) - MWIIW
HEp-2 (larynx, carcinoma, squamous cell) - PRUMB
Hep-2 (larynx, carcinoma, squamous cell) - RMSTC
HEp-2 (larynx, carcinoma, squamous cell) - SIUVI
HEp-2 (larynx, carcinoma, squamous cell) - SPBIC
Hep-2C (larynx, carcinoma) - ECACC
Hep2 (larynx, carcinoma) - ECACC
Hep2 (Clone 2B) (larynx, carcinoma) - ECACC
HFFF2 (foreskin, fetal) - ECACC
HFFF2 (foreskin, fetal) - ICLC
HG 261 (skin, fibroblast, Fanconi anemia) - IZSBS
HG261 (skin, fibroblast, Fanconi anemia) - ECACC
HK 0-32 (skin, keratinocyte) - MIUCO
HK 0-42 (skin, keratinocyte) - MIUCO
HK 0-43 (skin, keratinocyte) - MIUCO
HK 0-44 (skin, keratinocyte) - MIUCO
HK 0-45 (skin, keratinocyte) - MIUCO
HL 60 (peripheral blood, leukemia) - IZSBS
HL-60 (peripheral blood, leukemia, promyelocytic) - ANIIR
HL-60 (peripheral blood, leukemia, promyelocytic) - BOHIC
HL-60 (peripheral blood, leukemia, promyelocytic) - ICLC
HL-60 (peripheral blood, leukemia, promyelocytic) - MIISB
HL-60 (peripheral blood, leukemia, promyelocytic) - PNIOS
HL-60 (peripheral blood, leukemia, promyelocytic) - RMUFM
HL-60 (peripheral blood, leukemia, promyelocytic) - SPBIC
HL60 (peripheral blood, leukemia, promyelocytic) - ECACC
HL60 15-12 (peripheral blood, leukemia, promyelocytic) - ECACC
HL60 Ast.3 (peripheral blood, leukemia, promyelocytic) - ECACC
HL60 Ast.4 (peripheral blood, leukemia, promyelocytic) - ECACC
HL60 M2 (peripheral blood, leukemia, promyelocytic) - ECACC
HL60 M4 (blood, leukemia, promyelocytic) - ECACC
HOS (bone, osteosarcoma) - ECACC
HOS (bone, osteosarcoma) - ICLC
HOS (bone, osteosarcoma) - IZSBS
HOS (TE85, Clone F5) (bone, osteosarcoma) - MIISA
HOS (TE85, Clone F5) (bone, osteosarcoma) - MWIIW
HOS (TE85, Clone F5) (bone, osteosarcoma) - SPBIC
Hs 578Bst (breast) - MIEOS
Hs 578T (breast, carcinoma, ductal) - ECACC
Hs 578T (breast, carcinoma) - ICLC
Hs 578T (breast, carcinoma, ductal) - SPBIC
Hs 68 (foreskin) - ECACC
HS 888 Lu (lung) - IZSBS
Hs 888Lu (lung) - ECACC
HS-Sultan (blood, plasmacytoma) - ECACC
Hs913T (fibrosarcoma) - ICLC
HT 1080 (acetabulum, fibrosarcoma) - ECACC
HT 1080 (acetabulum, fibrosarcoma) - IZSBS
HT 1197 (bladder, carcinoma) - ECACC
HT 1197 (bladder, carcinoma) - ICLC
HT 1376 (bladder, carcinoma) - ECACC
HT 1376 (bladder, carcinoma) - IZSBS
HT-1080 (acetabulum, fibrosarcoma) - BGEBS
HT-1080 (acetabulum, fibrosarcoma) - CHIBC
HT-1080 (acetabulum, fibrosarcoma) - GEICH
HT-1080 (acetabulum, fibrosarcoma) - ICLC
HT-1080 (acetabulum, fibrosarcoma) - MIEOS
HT-1080 (acetabulum, fibrosarcoma) - SPBIC
HT-29 (colon, adenocarcinoma, grade II) - ICLC
HT-29 (colon, adenocarcinoma) - IZSBS
HT-29 (colon, adenocarcinoma, grade II) - MIEOS
HT-29 (colon, adenocarcinoma, grade II) - MIILC
HT-29 (colon, adenocarcinoma, grade II) - MIISB
HT-29 (colon, adenocarcinoma, grade II) - MWIIW
HT-29 (colon, adenocarcinoma, grade II) - RMICS
HT-29 (colon, adenocarcinoma, grade II) - TOUCI
HT29 (colon, adenocarcinoma, grade II) - ECACC
I-B92 (amnion, trisomy 21 / Down syndrome) - GGB
I-P94 (amnion, trisomy 21 / Down syndrome) - GGB
I1094 (fibroblast) - GGB
I1686 (fibroblast) - GGB
I2586 (fibroblast, achondrogenesis I) - GGB
IC86 (lymphocyte, trisomy 21 / Down syndrome) - GGB
IG88IL2 (lymphocyte) - GGB
IG88ls (lymphocyte) - GGB
IGA001/83 (amnion) - GEIMM
IGA001/85 (amnion, propionicacidemia I) - GEIMM
IGA001/92 (amnion, maple syrup urine disease) - GEIMM
IGA001/99 (amnion, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGA004/90 (amnion, glycogen storage disease II) - GEIMM
IGA004/95 (amnion, Krabbe disease) - GEIMM
IGA004/99 (amnion, methylmalonicacidemia) - GEIMM
IGA005/84 (amnion, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGA005/98 (amnion, methylmalonicacidemia) - GEIMM
IGA007/96 (amnion, mucolipidosis II) - GEIMM
IGA008/82 (amnion, glycogen storage disease II) - GEIMM
IGA009/84 (amnion, Niemann-Pick disease, type A) - GEIMM
IGA009/98 (amnion, mucolipidosis II) - GEIMM
IGA010/89 (amnion, Niemann-Pick disease, type A) - GEIMM
IGA013/83 (amnion, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGA015/96 (amnion, galactosemia) - GEIMM
IGA016/84 (amnion, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGA017/99 (amnion, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGA018/85 (amnion, Tay-Sachs disease) - GEIMM
IGA020/90 (amnion, metachromatic leukodystrophy, late-infantile) - GEIMM
IGA022/82 (amnion, fucosidosis) - GEIMM
IGA022/99 (amnion, Menkes syndrome) - GEIMM
IGA024/90 (amnion, Niemann-Pick disease, type A) - GEIMM
IGA028/83 (amnion, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGA031/82 (amnion, glycogen storage disease II) - GEIMM
IGA031/87 (amnion) - GEIMM
IGA033/83 (amnion, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGA036/83 (amnion, glycogen storage disease II) - GEIMM
IGA040/78 (amnion, fucosidosis) - GEIMM
IGA040/82 (amnion, propionicacidemia I) - GEIMM
IGA058/80 (amnion, glycogen storage disease II) - GEIMM
IGA063/80 (amnion, mucopolysaccharidosis type VI) - GEIMM
IGA188/78 (amnion, mannosidosis, alpha b, lysosomal) - GEIMM
IGF001/00 (skin, fibroblast) - GEIMM
IGF001/01 (skin, fibroblast) - GEIMM
IGF001/77 (skin, fibroblast) - GEIMM
IGF001/78 (skin, fibroblast, B1 variant - GM2 gangliosidosis / Tay-Sachs disease) - GEIMM
IGF001/80 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF001/81 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF001/83 (skin, fibroblast) - GEIMM
IGF001/84 (skin, fibroblast) - GEIMM
IGF001/85 (skin, fibroblast) - GEIMM
IGF001/86 (skin, fibroblast) - GEIMM
IGF001/87 (skin, fibroblast) - GEIMM
IGF001/90 (skin, fibroblast, Steinert disease) - GEIMM
IGF001/91 (skin, fibroblast, Charcot-Marie-Tooth disease) - GEIMM
IGF001/93 (skin, fibroblast) - GEIMM
IGF001/94 (skin, fibroblast, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF001/95 (skin, fibroblast) - GEIMM
IGF001/96 (skin, fibroblast, Wolman disease/cholesterol ester storage disease) - GEIMM
IGF001/97 (skin, fibroblast) - GEIMM
IGF001/98 (skin, fibroblast, Glutaricacidemia I) - GEIMM
IGF001/99 (skin, fibroblast) - GEIMM
IGF002/00 (skin, fibroblast, Krabbe disease) - GEIMM
IGF002/01 (skin, fibroblast) - GEIMM
IGF002/77 (skin, fibroblast) - GEIMM
IGF002/78 (skin, fibroblast, phenylketonuria II) - GEIMM
IGF002/79 (skin, fibroblast) - GEIMM
IGF002/80 (skin, fibroblast, Fanconi-Bickel syndrome) - GEIMM
IGF002/81 (skin, fibroblast) - GEIMM
IGF002/82 (skin, fibroblast) - GEIMM
IGF002/83 (skin, fibroblast) - GEIMM
IGF002/85 (skin, fibroblast, osteogenesis imperfecta) - GEIMM
IGF002/86 (skin, fibroblast) - GEIMM
IGF002/87 (skin, fibroblast) - GEIMM
IGF002/88 (skin, fibroblast, propionicacidemia I) - GEIMM
IGF002/90 (skin, fibroblast) - GEIMM
IGF002/91 (skin, fibroblast) - GEIMM
IGF002/92 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF002/93 (skin, fibroblast) - GEIMM
IGF002/94 (skin, fibroblast) - GEIMM
IGF002/95 (skin, fibroblast, McCune-Albright sindrome) - GEIMM
IGF002/96 (skin, fibroblast, DiGeorge syndrome) - GEIMM
IGF002/97 (skin, fibroblast) - GEIMM
IGF002/98 (skin, fibroblast) - GEIMM
IGF002/99 (skin, fibroblast) - GEIMM
IGF003/00 (skin, fibroblast) - GEIMM
IGF003/01 (skin, fibroblast) - GEIMM
IGF003/77 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF003/80 (skin, fibroblast) - GEIMM
IGF003/81 (skin, fibroblast) - GEIMM
IGF003/82 (skin, fibroblast, metatropic dwarfism, type II) - GEIMM
IGF003/83 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF003/85 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF003/86 (skin, fibroblast) - GEIMM
IGF003/87 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF003/88 (skin, fibroblast) - GEIMM
IGF003/89 (skin, fibroblast, Freeman-Sheldon syndrome) - GEIMM
IGF003/93 (skin, fibroblast) - GEIMM
IGF003/94 (skin, fibroblast) - GEIMM
IGF003/96 (skin, fibroblast) - GEIMM
IGF003/97 (skin, fibroblast) - GEIMM
IGF003/98 (skin, fibroblast) - GEIMM
IGF003/99 (skin, fibroblast) - GEIMM
IGF004/00 (skin, fibroblast, salla disease) - GEIMM
IGF004/01 (skin, fibroblast) - GEIMM
IGF004/78 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF004/79 (skin, fibroblast) - GEIMM
IGF004/81 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGF004/82 (skin, fibroblast) - GEIMM
IGF004/83 (skin, fibroblast) - GEIMM
IGF004/84 (skin, fibroblast, methylmalonicacidemia) - GEIMM
IGF004/85 (skin, fibroblast, Menkes syndrome) - GEIMM
IGF004/86 (skin, fibroblast) - GEIMM
IGF004/87 (skin, fibroblast) - GEIMM
IGF004/89 (skin, fibroblast, metatropic dwarfism, type II) - GEIMM
IGF004/91 (skin, fibroblast, Ehlers-Danlos syndrome, type IV, autosomal dominant) - GEIMM
IGF004/93 (skin, fibroblast) - GEIMM
IGF004/94 (skin, fibroblast) - GEIMM
IGF004/96 (skin, fibroblast, Cockayne syndrome) - GEIMM
IGF004/97 (skin, fibroblast) - GEIMM
IGF004/98 (skin, fibroblast, neuropathy, giant axonal) - GEIMM
IGF004/99 (skin, fibroblast) - GEIMM
IGF005/00 (skin, fibroblast) - GEIMM
IGF005/01 (skin, fibroblast) - GEIMM
IGF005/77 (skin, fibroblast) - GEIMM
IGF005/80 (skin, fibroblast) - GEIMM
IGF005/82 (skin, fibroblast) - GEIMM
IGF005/83 (skin, fibroblast) - GEIMM
IGF005/84 (skin, fibroblast, methylmalonicacidemia) - GEIMM
IGF005/85 (skin, fibroblast) - GEIMM
IGF005/86 (skin, fibroblast) - GEIMM
IGF005/87 (skin, fibroblast) - GEIMM
IGF005/89 (skin, fibroblast) - GEIMM
IGF005/91 (skin, fibroblast) - GEIMM
IGF005/92 (skin, fibroblast, NARP mutation) - GEIMM
IGF005/93 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF005/94 (skin, fibroblast) - GEIMM
IGF005/95 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGF005/96 (skin, fibroblast, mucopolysaccharidosis type III B) - GEIMM
IGF005/97 (skin, fibroblast) - GEIMM
IGF005/98 (skin, fibroblast, glycogen storage disease IV) - GEIMM
IGF005/99 (skin, fibroblast) - GEIMM
IGF006/00 (skin, fibroblast) - GEIMM
IGF006/01 (skin, fibroblast) - GEIMM
IGF006/77 (skin, fibroblast) - GEIMM
IGF006/79 (skin, fibroblast) - GEIMM
IGF006/80 (skin, fibroblast, camptomelic dwarfism) - GEIMM
IGF006/81 (skin, fibroblast) - GEIMM
IGF006/82 (skin, fibroblast, hypophosphatasia infantile) - GEIMM
IGF006/83 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF006/84 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF006/85 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF006/86 (skin, fibroblast) - GEIMM
IGF006/87 (skin, fibroblast) - GEIMM
IGF006/89 (skin, fibroblast) - GEIMM
IGF006/91 (skin, fibroblast) - GEIMM
IGF006/92 (skin, fibroblast, neuraminidase deficiency) - GEIMM
IGF006/93 (skin, fibroblast, homocystinuria - megaloblastic anemia) - GEIMM
IGF006/94 (skin, fibroblast, neuraminidase deficiency with beta-galactosidase deficiency) - GEIMM
IGF006/95 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF006/96 (skin, fibroblast) - GEIMM
IGF006/97 (skin, fibroblast) - GEIMM
IGF006/98 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF006/99 (skin, fibroblast) - GEIMM
IGF007/00 (skin, fibroblast) - GEIMM
IGF007/01 (skin, fibroblast) - GEIMM
IGF007/79 (skin, fibroblast) - GEIMM
IGF007/80 (skin, fibroblast) - GEIMM
IGF007/81 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF007/84 (skin, fibroblast) - GEIMM
IGF007/85 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF007/86 (skin, fibroblast) - GEIMM
IGF007/87 (skin, fibroblast) - GEIMM
IGF007/89 (skin, fibroblast, B1 variant - GM2 gangliosidosis / Tay-Sachs disease) - GEIMM
IGF007/90 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF007/91 (skin, fibroblast) - GEIMM
IGF007/92 (skin, fibroblast, Cockayne syndrome) - GEIMM
IGF007/93 (skin, fibroblast, mucopolysaccharidosis type III B) - GEIMM
IGF007/95 (skin, fibroblast) - GEIMM
IGF007/96 (skin, fibroblast) - GEIMM
IGF007/97 (skin, fibroblast) - GEIMM
IGF007/98 (skin, fibroblast, Davidson disease) - GEIMM
IGF007/99 (skin, fibroblast) - GEIMM
IGF008/00 (skin, fibroblast) - GEIMM
IGF008/01 (skin, fibroblast) - GEIMM
IGF008/78 (skin, fibroblast) - GEIMM
IGF008/79 (skin, fibroblast) - GEIMM
IGF008/80 (skin, fibroblast, neuraminidase deficiency) - GEIMM
IGF008/81 (skin, fibroblast) - GEIMM
IGF008/82 (skin, fibroblast, Gaucher disease type III) - GEIMM
IGF008/84 (skin, fibroblast, mucopolysaccharidosis type III C) - GEIMM
IGF008/86 (skin, fibroblast) - GEIMM
IGF008/87 (skin, fibroblast) - GEIMM
IGF008/88 (skin, fibroblast) - GEIMM
IGF008/89 (skin, fibroblast, osteogenesis imperfecta, type II) - GEIMM
IGF008/92 (skin, fibroblast) - GEIMM
IGF008/94 (skin, fibroblast) - GEIMM
IGF008/96 (skin, fibroblast) - GEIMM
IGF008/97 (skin, fibroblast) - GEIMM
IGF008/98 (skin, fibroblast) - GEIMM
IGF008/99 (skin, fibroblast) - GEIMM
IGF009/00 (skin, fibroblast) - GEIMM
IGF009/01 (skin, fibroblast) - GEIMM
IGF009/77 (skin, fibroblast, Gaucher disease type III) - GEIMM
IGF009/78 (skin, fibroblast) - GEIMM
IGF009/80 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF009/81 (skin, fibroblast, neuronal ceroid-lipofuscinosis infantile Finnish type) - GEIMM
IGF009/82 (skin, fibroblast) - GEIMM
IGF009/84 (skin, fibroblast, neuraminidase deficiency) - GEIMM
IGF009/85 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF009/86 (skin, fibroblast, mucopolysaccharidosis type III C) - GEIMM
IGF009/87 (skin, fibroblast) - GEIMM
IGF009/88 (skin, fibroblast) - GEIMM
IGF009/89 (skin, fibroblast, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF009/90 (skin, fibroblast, Zellweger syndrome) - GEIMM
IGF009/91 (skin, fibroblast) - GEIMM
IGF009/92 (skin, fibroblast) - GEIMM
IGF009/93 (skin, fibroblast, Krabbe disease) - GEIMM
IGF009/94 (skin, fibroblast) - GEIMM
IGF009/96 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF009/97 (skin, fibroblast) - GEIMM
IGF009/98 (skin, fibroblast, Pallister Killian syndrome) - GEIMM
IGF009/99 (skin, fibroblast) - GEIMM
IGF010/00 (skin, fibroblast) - GEIMM
IGF010/77 (skin, fibroblast, Sandhoff disease) - GEIMM
IGF010/78 (skin, fibroblast) - GEIMM
IGF010/80 (skin, fibroblast) - GEIMM
IGF010/81 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF010/83 (skin, fibroblast) - GEIMM
IGF010/84 (skin, fibroblast, B1 variant - GM2 gangliosidosis / Tay-Sachs disease) - GEIMM
IGF010/85 (skin, fibroblast) - GEIMM
IGF010/86 (skin, fibroblast) - GEIMM
IGF010/87 (skin, fibroblast) - GEIMM
IGF010/88 (skin, fibroblast) - GEIMM
IGF010/89 (skin, fibroblast) - GEIMM
IGF010/90 (skin, fibroblast, Wilson disease) - GEIMM
IGF010/91 (skin, fibroblast) - GEIMM
IGF010/92 (skin, fibroblast) - GEIMM
IGF010/93 (skin, fibroblast) - GEIMM
IGF010/94 (skin, fibroblast, Marfan syndrome) - GEIMM
IGF010/96 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF010/97 (skin, fibroblast) - GEIMM
IGF010/98 (skin, fibroblast) - GEIMM
IGF010/99 (skin, fibroblast) - GEIMM
IGF011/00 (skin, fibroblast) - GEIMM
IGF011/01 (skin, fibroblast) - GEIMM
IGF011/77 (skin, fibroblast, Ehlers-Danlos syndrome, type I) - GEIMM
IGF011/78 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF011/80 (skin, fibroblast) - GEIMM
IGF011/81 (skin, fibroblast, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF011/82 (skin, fibroblast, amaurotic family idiocy, juvenile type/neuronal ceroid lipofuscinosis) - GEIMM
IGF011/83 (skin, fibroblast) - GEIMM
IGF011/84 (skin, fibroblast) - GEIMM
IGF011/85 (skin, fibroblast) - GEIMM
IGF011/86 (skin, fibroblast) - GEIMM
IGF011/87 (skin, fibroblast) - GEIMM
IGF011/89 (skin, fibroblast) - GEIMM
IGF011/90 (skin, fibroblast) - GEIMM
IGF011/91 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF011/92 (skin, fibroblast, Ehlers-Danlos syndrome, type I) - GEIMM
IGF011/93 (skin, fibroblast) - GEIMM
IGF011/94 (skin, fibroblast) - GEIMM
IGF011/96 (skin, fibroblast, homocystinuria - megaloblastic anemia) - GEIMM
IGF011/97 (skin, fibroblast) - GEIMM
IGF011/98 (skin, fibroblast) - GEIMM
IGF011/99 (skin, fibroblast, osteopetrosis autosomal recessive) - GEIMM
IGF012/00 (skin, fibroblast) - GEIMM
IGF012/01 (skin, fibroblast) - GEIMM
IGF012/77 (skin, fibroblast) - GEIMM
IGF012/78 (skin, fibroblast) - GEIMM
IGF012/80 (skin, fibroblast) - GEIMM
IGF012/81 (skin, fibroblast, tyrosine transaminase deficiency) - GEIMM
IGF012/82 (skin, fibroblast) - GEIMM
IGF012/83 (skin, fibroblast) - GEIMM
IGF012/84 (skin, fibroblast) - GEIMM
IGF012/85 (skin, fibroblast, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF012/86 (skin, fibroblast) - GEIMM
IGF012/87 (skin, fibroblast, spondyloepiphyseal dysplasia, congenital) - GEIMM
IGF012/89 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF012/90 (skin, fibroblast, hydrocephalus, agyria, retinal dysplasia Hard syndrome/Walker-Warburg) - GEIMM
IGF012/91 (skin, fibroblast, Krabbe disease) - GEIMM
IGF012/92 (skin, fibroblast) - GEIMM
IGF012/93 (skin, fibroblast) - GEIMM
IGF012/94 (skin, fibroblast) - GEIMM
IGF012/96 (skin, fibroblast) - GEIMM
IGF012/98 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF012/99 (skin, fibroblast, Austin) - GEIMM
IGF013/00 (skin, fibroblast) - GEIMM
IGF013/01 (skin, fibroblast) - GEIMM
IGF013/77 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF013/78 (skin, fibroblast) - GEIMM
IGF013/80 (skin, fibroblast) - GEIMM
IGF013/81 (skin, fibroblast, tyrosine transaminase deficiency) - GEIMM
IGF013/82 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF013/84 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF013/85 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF013/86 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF013/87 (skin, fibroblast) - GEIMM
IGF013/89 (skin, fibroblast) - GEIMM
IGF013/90 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF013/91 (skin, fibroblast) - GEIMM
IGF013/92 (skin, fibroblast) - GEIMM
IGF013/93 (skin, fibroblast) - GEIMM
IGF013/94 (skin, fibroblast) - GEIMM
IGF013/95 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF013/96 (skin, fibroblast) - GEIMM
IGF013/99 (skin, fibroblast, sulfatidosis, juvenile, Austin type) - GEIMM
IGF014/00 (skin, fibroblast) - GEIMM
IGF014/01 (skin, fibroblast) - GEIMM
IGF014/78 (skin, fibroblast) - GEIMM
IGF014/80 (skin, fibroblast) - GEIMM
IGF014/81 (skin, fibroblast) - GEIMM
IGF014/82 (skin, fibroblast) - GEIMM
IGF014/83 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF014/84 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF014/85 (skin, fibroblast) - GEIMM
IGF014/86 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF014/87 (skin, fibroblast) - GEIMM
IGF014/89 (skin, fibroblast, Menkes syndrome) - GEIMM
IGF014/90 (skin, fibroblast, osteoporosis-pseudoglioma syndrome) - GEIMM
IGF014/91 (skin, fibroblast, Lesch-Nyhan syndrome) - GEIMM
IGF014/92 (skin, fibroblast) - GEIMM
IGF014/93 (skin, fibroblast) - GEIMM
IGF014/94 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF014/95 (skin, fibroblast) - GEIMM
IGF014/96 (skin, fibroblast) - GEIMM
IGF014/97 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF014/98 (skin, fibroblast) - GEIMM
IGF014/99 (skin, fibroblast) - GEIMM
IGF015/00 (skin, fibroblast) - GEIMM
IGF015/01 (skin, fibroblast) - GEIMM
IGF015/78 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGF015/80 (skin, fibroblast) - GEIMM
IGF015/82 (skin, fibroblast) - GEIMM
IGF015/83 (skin, fibroblast) - GEIMM
IGF015/84 (skin, fibroblast, mucopolysaccharidosis type III B) - GEIMM
IGF015/85 (skin, fibroblast) - GEIMM
IGF015/86 (skin, fibroblast) - GEIMM
IGF015/87 (skin, fibroblast) - GEIMM
IGF015/90 (skin, fibroblast, osteoporosis-pseudoglioma syndrome) - GEIMM
IGF015/91 (skin, fibroblast) - GEIMM
IGF015/94 (skin, fibroblast) - GEIMM
IGF015/95 (skin, fibroblast, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF015/96 (skin, fibroblast, osteogenesis imperfecta) - GEIMM
IGF015/97 (skin, fibroblast, def. PDH complex thiamine responsive) - GEIMM
IGF015/98 (skin, fibroblast) - GEIMM
IGF015/99 (skin, fibroblast) - GEIMM
IGF016/00 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF016/01 (skin, fibroblast) - GEIMM
IGF016/77 (skin, fibroblast, cystic fibrosis) - GEIMM
IGF016/78 (skin, fibroblast, Ehlers-Danlos syndrome) - GEIMM
IGF016/80 (skin, fibroblast) - GEIMM
IGF016/81 (skin, fibroblast) - GEIMM
IGF016/82 (skin, fibroblast, tyrosine transaminase deficiency) - GEIMM
IGF016/83 (skin, fibroblast, adrenoleukodystrophy / addison disease and cerebral sclerosis) - GEIMM
IGF016/84 (skin, fibroblast) - GEIMM
IGF016/85 (skin, fibroblast) - GEIMM
IGF016/86 (skin, fibroblast, Marinesco-Sjogren syndrome) - GEIMM
IGF016/87 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF016/89 (skin, fibroblast) - GEIMM
IGF016/90 (skin, fibroblast) - GEIMM
IGF016/91 (skin, fibroblast) - GEIMM
IGF016/92 (skin, fibroblast) - GEIMM
IGF016/93 (skin, fibroblast) - GEIMM
IGF016/94 (skin, fibroblast) - GEIMM
IGF016/95 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGF016/96 (skin, fibroblast, Krabbe disease) - GEIMM
IGF016/97 (skin, fibroblast) - GEIMM
IGF016/98 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF016/99 (skin, fibroblast) - GEIMM
IGF017/00 (skin, fibroblast, mucopolysaccharidosis type III D) - GEIMM
IGF017/01 (skin, fibroblast) - GEIMM
IGF017/76 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF017/78 (skin, fibroblast, gangliosidosis, generalized GM1, type II) - GEIMM
IGF017/80 (skin, fibroblast) - GEIMM
IGF017/82 (skin, fibroblast, tyrosine transaminase deficiency) - GEIMM
IGF017/83 (skin, fibroblast) - GEIMM
IGF017/84 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF017/85 (skin, fibroblast) - GEIMM
IGF017/86 (skin, fibroblast) - GEIMM
IGF017/87 (skin, fibroblast) - GEIMM
IGF017/89 (skin, fibroblast) - GEIMM
IGF017/90 (skin, fibroblast, osteogenesis imperfecta, type II) - GEIMM
IGF017/91 (skin, fibroblast) - GEIMM
IGF017/92 (skin, fibroblast, Costello syndrome) - GEIMM
IGF017/93 (skin, fibroblast) - GEIMM
IGF017/95 (skin, fibroblast, leukoencephalopathy with vanishing white matter) - GEIMM
IGF017/96 (skin, fibroblast) - GEIMM
IGF017/97 (skin, fibroblast) - GEIMM
IGF017/98 (skin, fibroblast) - GEIMM
IGF017/99 (skin, fibroblast) - GEIMM
IGF018/00 (skin, fibroblast, X duplication) - GEIMM
IGF018/01 (skin, fibroblast) - GEIMM
IGF018/77 (skin, fibroblast, mucopolysaccharidosis type III D) - GEIMM
IGF018/78 (skin, fibroblast, Sandhoff disease) - GEIMM
IGF018/80 (skin, fibroblast) - GEIMM
IGF018/81 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF018/82 (skin, fibroblast) - GEIMM
IGF018/83 (skin, fibroblast, Sandhoff disease) - GEIMM
IGF018/84 (skin, fibroblast) - GEIMM
IGF018/85 (skin, fibroblast, Gaucher disease type II) - GEIMM
IGF018/86 (skin, fibroblast) - GEIMM
IGF018/87 (skin, fibroblast) - GEIMM
IGF018/88 (skin, fibroblast) - GEIMM
IGF018/89 (skin, fibroblast) - GEIMM
IGF018/90 (skin, fibroblast, complex IV,mitocondrial respiratory chain,deficiency of) - GEIMM
IGF018/91 (skin, fibroblast) - GEIMM
IGF018/92 (skin, fibroblast) - GEIMM
IGF018/93 (skin, fibroblast, osteogenesis imperfecta, type II) - GEIMM
IGF018/94 (skin, fibroblast, Krabbe disease) - GEIMM
IGF018/95 (skin, fibroblast) - GEIMM
IGF018/96 (skin, fibroblast) - GEIMM
IGF018/97 (skin, fibroblast) - GEIMM
IGF018/98 (skin, fibroblast) - GEIMM
IGF018/99 (skin, fibroblast) - GEIMM
IGF019/00 (skin, fibroblast) - GEIMM
IGF019/01 (skin, fibroblast) - GEIMM
IGF019/77 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF019/78 (skin, fibroblast) - GEIMM
IGF019/80 (skin, fibroblast, neuroaxonal dystrophy, infantile) - GEIMM
IGF019/82 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF019/84 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF019/85 (skin, fibroblast) - GEIMM
IGF019/86 (skin, fibroblast) - GEIMM
IGF019/87 (skin, fibroblast, ataxia telangiectasia) - GEIMM
IGF019/88 (skin, fibroblast) - GEIMM
IGF019/89 (skin, fibroblast) - GEIMM
IGF019/90 (skin, fibroblast, osteogenesis imperfecta) - GEIMM
IGF019/91 (skin, fibroblast) - GEIMM
IGF019/92 (skin, fibroblast) - GEIMM
IGF019/93 (skin, fibroblast, homocystinuria - megaloblastic anemia) - GEIMM
IGF019/96 (skin, fibroblast, acyl-CoA dehydrogenase, long-chain, deficiency) - GEIMM
IGF019/97 (skin, fibroblast) - GEIMM
IGF019/98 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF019/99 (skin, fibroblast) - GEIMM
IGF020/00 (skin, fibroblast, SURF1) - GEIMM
IGF020/01 (skin, fibroblast) - GEIMM
IGF020/78 (skin, fibroblast) - GEIMM
IGF020/80 (skin, fibroblast) - GEIMM
IGF020/82 (skin, fibroblast) - GEIMM
IGF020/83 (skin, fibroblast, multiple carboxylase deficiency, late-onset) - GEIMM
IGF020/84 (skin, fibroblast, Krabbe disease) - GEIMM
IGF020/85 (skin, fibroblast) - GEIMM
IGF020/86 (skin, fibroblast) - GEIMM
IGF020/87 (skin, fibroblast) - GEIMM
IGF020/88 (skin, fibroblast) - GEIMM
IGF020/89 (skin, fibroblast) - GEIMM
IGF020/90 (skin, fibroblast) - GEIMM
IGF020/91 (skin, fibroblast) - GEIMM
IGF020/92 (skin, fibroblast) - GEIMM
IGF020/93 (skin, fibroblast, Krabbe disease) - GEIMM
IGF020/94 (skin, fibroblast, homocystinuria - megaloblastic anemia) - GEIMM
IGF020/95 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF020/96 (skin, fibroblast, proteolipid protein, myelin) - GEIMM
IGF020/97 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF020/98 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF020/99 (skin, fibroblast) - GEIMM
IGF021/00 (skin, fibroblast) - GEIMM
IGF021/01 (skin, fibroblast) - GEIMM
IGF021/78 (skin, fibroblast) - GEIMM
IGF021/82 (skin, fibroblast) - GEIMM
IGF021/83 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF021/84 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF021/85 (skin, fibroblast) - GEIMM
IGF021/86 (skin, fibroblast, Kartagener syndrome X) - GEIMM
IGF021/87 (skin, fibroblast, complex IV,mitocondrial respiratory chain,deficiency of) - GEIMM
IGF021/88 (skin, fibroblast) - GEIMM
IGF021/90 (skin, fibroblast) - GEIMM
IGF021/91 (skin, fibroblast) - GEIMM
IGF021/92 (skin, fibroblast) - GEIMM
IGF021/93 (skin, fibroblast) - GEIMM
IGF021/94 (skin, fibroblast, fructose-1, 6-diphosphatase deficiency) - GEIMM
IGF021/95 (skin, fibroblast) - GEIMM
IGF021/96 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF021/97 (skin, fibroblast) - GEIMM
IGF021/98 (skin, fibroblast) - GEIMM
IGF021/99 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF022/00 (skin, fibroblast) - GEIMM
IGF022/01 (skin, fibroblast) - GEIMM
IGF022/77 (skin, fibroblast) - GEIMM
IGF022/78 (skin, fibroblast) - GEIMM
IGF022/79 (skin, fibroblast) - GEIMM
IGF022/80 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF022/81 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF022/82 (skin, fibroblast) - GEIMM
IGF022/83 (skin, fibroblast) - GEIMM
IGF022/84 (skin, fibroblast) - GEIMM
IGF022/85 (skin, fibroblast) - GEIMM
IGF022/86 (skin, fibroblast, Sandhoff disease) - GEIMM
IGF022/87 (skin, fibroblast, Lesch-Nyhan syndrome) - GEIMM
IGF022/88 (skin, fibroblast) - GEIMM
IGF022/89 (skin, fibroblast, spinal muscolar atrophy I / Werdnig-Hoffmann disease) - GEIMM
IGF022/90 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF022/91 (skin, fibroblast) - GEIMM
IGF022/92 (skin, fibroblast) - GEIMM
IGF022/93 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF022/94 (skin, fibroblast, methylmalonicacidemia) - GEIMM
IGF022/95 (skin, fibroblast) - GEIMM
IGF022/96 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF022/97 (skin, fibroblast) - GEIMM
IGF022/98 (skin, fibroblast) - GEIMM
IGF022/99 (skin, fibroblast) - GEIMM
IGF023/00 (skin, fibroblast) - GEIMM
IGF023/01 (skin, fibroblast) - GEIMM
IGF023/77 (skin, fibroblast) - GEIMM
IGF023/78 (skin, fibroblast) - GEIMM
IGF023/79 (skin, fibroblast) - GEIMM
IGF023/81 (skin, fibroblast) - GEIMM
IGF023/83 (skin, fibroblast, Fanconi-Bickel syndrome) - GEIMM
IGF023/84 (skin, fibroblast, Engelmann disease) - GEIMM
IGF023/85 (skin, fibroblast, glycogen storage disease III) - GEIMM
IGF023/86 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF023/87 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF023/88 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF023/90 (skin, fibroblast) - GEIMM
IGF023/91 (skin, fibroblast) - GEIMM
IGF023/93 (skin, fibroblast) - GEIMM
IGF023/94 (skin, fibroblast) - GEIMM
IGF023/95 (skin, fibroblast) - GEIMM
IGF023/96 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF023/97 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF023/98 (skin, fibroblast) - GEIMM
IGF023/99 (skin, fibroblast) - GEIMM
IGF024/00 (skin, fibroblast, citrullinemia) - GEIMM
IGF024/01 (skin, fibroblast) - GEIMM
IGF024/77 (skin, fibroblast, neuraminidase deficiency) - GEIMM
IGF024/78 (skin, fibroblast) - GEIMM
IGF024/79 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF024/81 (skin, fibroblast, dibasicaminoaciduria II) - GEIMM
IGF024/82 (skin, fibroblast) - GEIMM
IGF024/83 (skin, fibroblast) - GEIMM
IGF024/85 (skin, fibroblast, glycogen storage disease III) - GEIMM
IGF024/86 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF024/88 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF024/90 (skin, fibroblast) - GEIMM
IGF024/91 (skin, fibroblast) - GEIMM
IGF024/92 (skin, fibroblast) - GEIMM
IGF024/93 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF024/94 (skin, fibroblast) - GEIMM
IGF024/95 (skin, fibroblast) - GEIMM
IGF024/96 (skin, fibroblast) - GEIMM
IGF024/97 (skin, fibroblast) - GEIMM
IGF024/98 (skin, fibroblast) - GEIMM
IGF024/99 (skin, fibroblast) - GEIMM
IGF025/00 (skin, fibroblast) - GEIMM
IGF025/01 (skin, fibroblast) - GEIMM
IGF025/77 (skin, fibroblast, neuraminidase deficiency) - GEIMM
IGF025/78 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF025/80 (skin, fibroblast) - GEIMM
IGF025/81 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF025/82 (skin, fibroblast, mucopolysaccharidosis type III C) - GEIMM
IGF025/83 (skin, fibroblast) - GEIMM
IGF025/84 (skin, fibroblast) - GEIMM
IGF025/85 (skin, fibroblast, adrenoleukodystrophy / addison disease and cerebral sclerosis) - GEIMM
IGF025/86 (skin, fibroblast) - GEIMM
IGF025/87 (skin, fibroblast) - GEIMM
IGF025/88 (skin, fibroblast, mucopolysaccharidosis type VI) - GEIMM
IGF025/89 (skin, fibroblast, Krabbe disease) - GEIMM
IGF025/90 (skin, fibroblast) - GEIMM
IGF025/91 (skin, fibroblast, acyl-CoA dehydrogenase, long-chain, deficiency) - GEIMM
IGF025/92 (skin, fibroblast, arthrogryposis multiplex congenita) - GEIMM
IGF025/93 (skin, fibroblast) - GEIMM
IGF025/95 (skin, fibroblast, fucosidosis) - GEIMM
IGF025/96 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF025/97 (skin, fibroblast) - GEIMM
IGF025/98 (skin, fibroblast, cystic fibrosis) - GEIMM
IGF025/99 (skin, fibroblast, Gaucher disease type II) - GEIMM
IGF026/00 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF026/01 (skin, fibroblast) - GEIMM
IGF026/77 (skin, fibroblast) - GEIMM
IGF026/78 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF026/80 (skin, fibroblast) - GEIMM
IGF026/82 (skin, fibroblast) - GEIMM
IGF026/83 (skin, fibroblast) - GEIMM
IGF026/84 (skin, fibroblast) - GEIMM
IGF026/85 (skin, fibroblast) - GEIMM
IGF026/86 (skin, fibroblast, Gaucher disease type III) - GEIMM
IGF026/87 (skin, fibroblast) - GEIMM
IGF026/88 (skin, fibroblast, neuraminidase deficiency) - GEIMM
IGF026/89 (skin, fibroblast) - GEIMM
IGF026/90 (skin, fibroblast, amaurotic family idiocy, late infantile type/NCL late infantile) - GEIMM
IGF026/91 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF026/92 (skin, fibroblast) - GEIMM
IGF026/93 (skin, fibroblast) - GEIMM
IGF026/95 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF026/96 (skin, fibroblast) - GEIMM
IGF026/97 (skin, fibroblast) - GEIMM
IGF026/98 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF026/99 (skin, fibroblast, Gaucher disease type II) - GEIMM
IGF027/00 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF027/01 (skin, fibroblast) - GEIMM
IGF027/77 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF027/78 (skin, fibroblast) - GEIMM
IGF027/80 (skin, fibroblast) - GEIMM
IGF027/82 (skin, fibroblast) - GEIMM
IGF027/83 (skin, fibroblast, mucopolysaccharidosis type III B) - GEIMM
IGF027/84 (skin, fibroblast) - GEIMM
IGF027/85 (skin, fibroblast) - GEIMM
IGF027/86 (skin, fibroblast) - GEIMM
IGF027/87 (skin, fibroblast) - GEIMM
IGF027/88 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF027/89 (skin, fibroblast) - GEIMM
IGF027/90 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF027/91 (skin, fibroblast) - GEIMM
IGF027/92 (skin, fibroblast) - GEIMM
IGF027/93 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF027/94 (skin, fibroblast) - GEIMM
IGF027/95 (skin, fibroblast, mucopolysaccharidosis type III B) - GEIMM
IGF027/96 (skin, fibroblast) - GEIMM
IGF027/97 (skin, fibroblast) - GEIMM
IGF027/98 (skin, fibroblast) - GEIMM
IGF027/99 (skin, fibroblast) - GEIMM
IGF028/00 (skin, fibroblast, spongy degeneration of central nervous system /Canavan disease) - GEIMM
IGF028/01 (skin, fibroblast) - GEIMM
IGF028/77 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF028/78 (skin, fibroblast) - GEIMM
IGF028/80 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF028/81 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF028/82 (skin, fibroblast, mucopolysaccharidosis type III B) - GEIMM
IGF028/83 (skin, fibroblast) - GEIMM
IGF028/84 (skin, fibroblast) - GEIMM
IGF028/85 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF028/86 (skin, fibroblast) - GEIMM
IGF028/87 (skin, fibroblast) - GEIMM
IGF028/88 (skin, fibroblast) - GEIMM
IGF028/89 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGF028/91 (skin, fibroblast) - GEIMM
IGF028/92 (skin, fibroblast, sialic acid storage disease) - GEIMM
IGF028/93 (skin, fibroblast) - GEIMM
IGF028/95 (skin, fibroblast, methylmalonicacidemia) - GEIMM
IGF028/97 (skin, fibroblast) - GEIMM
IGF028/98 (skin, fibroblast, Krabbe disease) - GEIMM
IGF028/99 (skin, fibroblast) - GEIMM
IGF029/00 (skin, fibroblast) - GEIMM
IGF029/01 (skin, fibroblast) - GEIMM
IGF029/77 (skin, fibroblast, arsa pseudodeficiency) - GEIMM
IGF029/78 (skin, fibroblast) - GEIMM
IGF029/81 (skin, fibroblast, homocystinuria) - GEIMM
IGF029/82 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF029/83 (skin, fibroblast, arsa pseudodeficiency) - GEIMM
IGF029/85 (skin, fibroblast, gangliosidosis, generalized GM1, type II) - GEIMM
IGF029/86 (skin, fibroblast) - GEIMM
IGF029/87 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF029/88 (skin, fibroblast) - GEIMM
IGF029/89 (skin, fibroblast) - GEIMM
IGF029/91 (skin, fibroblast) - GEIMM
IGF029/92 (skin, fibroblast, spastic paraparesis) - GEIMM
IGF029/93 (skin, fibroblast, methylmalonicacidemia) - GEIMM
IGF029/97 (skin, fibroblast) - GEIMM
IGF029/98 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF029/99 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF030/00 (skin, fibroblast) - GEIMM
IGF030/01 (skin, fibroblast) - GEIMM
IGF030/77 (skin, fibroblast) - GEIMM
IGF030/78 (skin, fibroblast) - GEIMM
IGF030/80 (skin, fibroblast) - GEIMM
IGF030/83 (skin, fibroblast) - GEIMM
IGF030/84 (skin, fibroblast) - GEIMM
IGF030/85 (skin, fibroblast) - GEIMM
IGF030/86 (skin, fibroblast) - GEIMM
IGF030/87 (skin, fibroblast) - GEIMM
IGF030/88 (skin, fibroblast) - GEIMM
IGF030/89 (skin, fibroblast) - GEIMM
IGF030/91 (skin, fibroblast) - GEIMM
IGF030/92 (skin, fibroblast) - GEIMM
IGF030/94 (skin, fibroblast) - GEIMM
IGF030/96 (skin, fibroblast) - GEIMM
IGF030/97 (skin, fibroblast) - GEIMM
IGF030/98 (skin, fibroblast) - GEIMM
IGF030/99 (skin, fibroblast) - GEIMM
IGF031/00 (skin, fibroblast, SURF1) - GEIMM
IGF031/01 (skin, fibroblast) - GEIMM
IGF031/77 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF031/80 (skin, fibroblast, mucopolysaccharidosis type III D) - GEIMM
IGF031/81 (skin, fibroblast) - GEIMM
IGF031/83 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF031/84 (skin, fibroblast) - GEIMM
IGF031/85 (skin, fibroblast, alkaptonuria) - GEIMM
IGF031/86 (skin, fibroblast) - GEIMM
IGF031/88 (skin, fibroblast) - GEIMM
IGF031/89 (skin, fibroblast) - GEIMM
IGF031/90 (skin, fibroblast, osteogenesis imperfecta, type I neurofibr.) - GEIMM
IGF031/91 (skin, fibroblast) - GEIMM
IGF031/92 (skin, fibroblast) - GEIMM
IGF031/93 (skin, fibroblast) - GEIMM
IGF031/94 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF031/96 (skin, fibroblast, Gaucher disease type II) - GEIMM
IGF031/97 (skin, fibroblast, Menkes syndrome) - GEIMM
IGF031/98 (skin, fibroblast) - GEIMM
IGF031/99 (skin, fibroblast) - GEIMM
IGF032/00 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF032/01 (skin, fibroblast) - GEIMM
IGF032/76 (skin, fibroblast, neuraminidase deficiency with beta-galactosidase deficiency) - GEIMM
IGF032/77 (skin, fibroblast) - GEIMM
IGF032/78 (skin, fibroblast) - GEIMM
IGF032/80 (skin, fibroblast) - GEIMM
IGF032/81 (skin, fibroblast, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF032/82 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF032/83 (skin, fibroblast, maple syrup urine disease) - GEIMM
IGF032/84 (skin, fibroblast) - GEIMM
IGF032/85 (skin, fibroblast, amaurotic family idiocy, late infantile type/NCL late infantile) - GEIMM
IGF032/86 (skin, fibroblast) - GEIMM
IGF032/87 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF032/88 (skin, fibroblast) - GEIMM
IGF032/89 (skin, fibroblast) - GEIMM
IGF032/90 (skin, fibroblast) - GEIMM
IGF032/91 (skin, fibroblast) - GEIMM
IGF032/93 (skin, fibroblast) - GEIMM
IGF032/94 (skin, fibroblast, osteogenesis imperfecta) - GEIMM
IGF032/96 (skin, fibroblast) - GEIMM
IGF032/97 (skin, fibroblast) - GEIMM
IGF032/98 (skin, fibroblast) - GEIMM
IGF032/99 (skin, fibroblast) - GEIMM
IGF033/00 (skin, fibroblast) - GEIMM
IGF033/01 (skin, fibroblast) - GEIMM
IGF033/77 (skin, fibroblast) - GEIMM
IGF033/78 (skin, fibroblast, Sandhoff disease) - GEIMM
IGF033/80 (skin, fibroblast) - GEIMM
IGF033/81 (skin, fibroblast, mucopolysaccharidosis type III B) - GEIMM
IGF033/83 (skin, fibroblast, fucosidosis) - GEIMM
IGF033/84 (skin, fibroblast) - GEIMM
IGF033/85 (skin, fibroblast) - GEIMM
IGF033/86 (skin, fibroblast, multiple carboxylase deficiency, biotin-responsive) - GEIMM
IGF033/87 (skin, fibroblast) - GEIMM
IGF033/88 (skin, fibroblast) - GEIMM
IGF033/89 (skin, fibroblast, sensorineural deafness) - GEIMM
IGF033/90 (skin, fibroblast, COFS syndrome / cerebrooculofacioskeletal syndrome) - GEIMM
IGF033/91 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF033/93 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF033/94 (skin, fibroblast) - GEIMM
IGF033/95 (skin, fibroblast) - GEIMM
IGF033/96 (skin, fibroblast) - GEIMM
IGF033/97 (skin, fibroblast, propionicacidemia I) - GEIMM
IGF033/98 (skin, fibroblast) - GEIMM
IGF033/99 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF034/00 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF034/01 (skin, fibroblast) - GEIMM
IGF034/76 (skin, fibroblast, SCID (severe combined immunodeficiency 1)) - GEIMM
IGF034/77 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGF034/80 (skin, fibroblast) - GEIMM
IGF034/81 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF034/83 (skin, fibroblast) - GEIMM
IGF034/84 (skin, fibroblast) - GEIMM
IGF034/85 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF034/86 (skin, fibroblast) - GEIMM
IGF034/87 (skin, fibroblast) - GEIMM
IGF034/88 (skin, fibroblast) - GEIMM
IGF034/89 (skin, fibroblast) - GEIMM
IGF034/90 (skin, fibroblast) - GEIMM
IGF034/91 (skin, fibroblast, B1 variant - GM2 gangliosidosis / Tay-Sachs disease) - GEIMM
IGF034/92 (skin, fibroblast) - GEIMM
IGF034/93 (skin, fibroblast) - GEIMM
IGF034/94 (skin, fibroblast) - GEIMM
IGF034/95 (skin, fibroblast) - GEIMM
IGF034/96 (skin, fibroblast) - GEIMM
IGF034/97 (skin, fibroblast, argininosuccinicaciduria) - GEIMM
IGF034/98 (skin, fibroblast) - GEIMM
IGF034/99 (skin, fibroblast) - GEIMM
IGF035/00 (skin, fibroblast) - GEIMM
IGF035/01 (skin, fibroblast) - GEIMM
IGF035/77 (skin, fibroblast, Niemann-Pick disease, type B) - GEIMM
IGF035/80 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF035/81 (skin, fibroblast, fucosidosis) - GEIMM
IGF035/82 (skin, fibroblast) - GEIMM
IGF035/83 (skin, fibroblast) - GEIMM
IGF035/85 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF035/86 (skin, fibroblast) - GEIMM
IGF035/87 (skin, fibroblast, gangliosidosis, generalized GM1, type II) - GEIMM
IGF035/88 (skin, fibroblast, fucosidosis) - GEIMM
IGF035/89 (skin, fibroblast) - GEIMM
IGF035/90 (skin, fibroblast) - GEIMM
IGF035/91 (skin, fibroblast) - GEIMM
IGF035/92 (skin, fibroblast, Menkes syndrome) - GEIMM
IGF035/93 (skin, fibroblast) - GEIMM
IGF035/94 (skin, fibroblast, mucolipidosis III) - GEIMM
IGF035/96 (skin, fibroblast) - GEIMM
IGF035/97 (skin, fibroblast) - GEIMM
IGF035/98 (skin, fibroblast) - GEIMM
IGF035/99 (skin, fibroblast) - GEIMM
IGF036/00 (skin, fibroblast, Krabbe disease) - GEIMM
IGF036/01 (skin, fibroblast) - GEIMM
IGF036/76 (skin, fibroblast) - GEIMM
IGF036/77 (skin, fibroblast) - GEIMM
IGF036/78 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF036/79 (skin, fibroblast, cystic fibrosis) - GEIMM
IGF036/80 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF036/81 (skin, fibroblast) - GEIMM
IGF036/83 (skin, fibroblast, Krabbe disease) - GEIMM
IGF036/84 (skin, fibroblast) - GEIMM
IGF036/86 (skin, fibroblast) - GEIMM
IGF036/87 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF036/88 (skin, fibroblast, osteogenesis imperfecta, type II) - GEIMM
IGF036/89 (skin, fibroblast) - GEIMM
IGF036/90 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF036/92 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF036/93 (skin, fibroblast) - GEIMM
IGF036/94 (skin, fibroblast) - GEIMM
IGF036/96 (skin, fibroblast) - GEIMM
IGF036/97 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF036/98 (skin, fibroblast) - GEIMM
IGF036/99 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF037/00 (skin, fibroblast) - GEIMM
IGF037/01 (skin, fibroblast) - GEIMM
IGF037/76 (skin, fibroblast) - GEIMM
IGF037/77 (skin, fibroblast) - GEIMM
IGF037/78 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF037/80 (skin, fibroblast) - GEIMM
IGF037/82 (skin, fibroblast) - GEIMM
IGF037/83 (skin, fibroblast) - GEIMM
IGF037/84 (skin, fibroblast, adrenoleukodystrophy / addison disease and cerebral sclerosis) - GEIMM
IGF037/85 (skin, fibroblast) - GEIMM
IGF037/86 (skin, fibroblast, myopathy with deficiency of CPT I) - GEIMM
IGF037/87 (skin, fibroblast) - GEIMM
IGF037/91 (skin, fibroblast) - GEIMM
IGF037/92 (skin, fibroblast) - GEIMM
IGF037/93 (skin, fibroblast) - GEIMM
IGF037/94 (skin, fibroblast, aspartylglycosaminuria) - GEIMM
IGF037/95 (skin, fibroblast, molybdenum cofactor deficiency) - GEIMM
IGF037/97 (skin, fibroblast, Sandhoff disease) - GEIMM
IGF037/99 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF038/00 (skin, fibroblast) - GEIMM
IGF038/01 (skin, fibroblast) - GEIMM
IGF038/80 (skin, fibroblast, Niemann-Pick disease, type B) - GEIMM
IGF038/81 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF038/82 (skin, fibroblast) - GEIMM
IGF038/83 (skin, fibroblast) - GEIMM
IGF038/84 (skin, fibroblast) - GEIMM
IGF038/85 (skin, fibroblast) - GEIMM
IGF038/86 (skin, fibroblast, Roberts syndrome) - GEIMM
IGF038/87 (skin, fibroblast) - GEIMM
IGF038/88 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGF038/89 (skin, fibroblast, isovalericacidemia) - GEIMM
IGF038/90 (skin, fibroblast) - GEIMM
IGF038/91 (skin, fibroblast, Charcot-Marie-Tooth disease) - GEIMM
IGF038/92 (skin, fibroblast) - GEIMM
IGF038/93 (skin, fibroblast, Turner syndrome, mosaic) - GEIMM
IGF038/95 (skin, fibroblast, encephalomyopaty mitocondrial) - GEIMM
IGF038/96 (skin, fibroblast, Gaucher disease type II) - GEIMM
IGF038/97 (skin, fibroblast) - GEIMM
IGF038/98 (skin, fibroblast) - GEIMM
IGF038/99 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF039/00 (skin, fibroblast) - GEIMM
IGF039/01 (skin, fibroblast) - GEIMM
IGF039/77 (skin, fibroblast) - GEIMM
IGF039/80 (skin, fibroblast) - GEIMM
IGF039/81 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF039/82 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF039/83 (skin, fibroblast) - GEIMM
IGF039/84 (skin, fibroblast) - GEIMM
IGF039/85 (skin, fibroblast, Ehlers-Danlos syndrome) - GEIMM
IGF039/86 (skin, fibroblast) - GEIMM
IGF039/87 (skin, fibroblast) - GEIMM
IGF039/88 (skin, fibroblast) - GEIMM
IGF039/90 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF039/91 (skin, fibroblast, Angelman syndrome) - GEIMM
IGF039/92 (skin, fibroblast) - GEIMM
IGF039/93 (skin, fibroblast, histiocytosis X) - GEIMM
IGF039/94 (skin, fibroblast) - GEIMM
IGF039/95 (skin, fibroblast) - GEIMM
IGF039/96 (skin, fibroblast) - GEIMM
IGF039/97 (skin, fibroblast) - GEIMM
IGF039/98 (skin, fibroblast) - GEIMM
IGF039/99 (skin, fibroblast, mucopolysaccharidosis type III C) - GEIMM
IGF040/00 (skin, fibroblast) - GEIMM
IGF040/01 (skin, fibroblast) - GEIMM
IGF040/77 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF040/78 (skin, fibroblast) - GEIMM
IGF040/79 (skin, fibroblast) - GEIMM
IGF040/80 (skin, fibroblast) - GEIMM
IGF040/82 (skin, fibroblast) - GEIMM
IGF040/83 (skin, fibroblast) - GEIMM
IGF040/84 (skin, fibroblast) - GEIMM
IGF040/85 (skin, fibroblast, Niemann-Pick disease, type B) - GEIMM
IGF040/86 (skin, fibroblast) - GEIMM
IGF040/87 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGF040/89 (skin, fibroblast, mucopolysaccharidosis type III B) - GEIMM
IGF040/90 (skin, fibroblast, Krabbe disease) - GEIMM
IGF040/91 (skin, fibroblast) - GEIMM
IGF040/92 (skin, fibroblast) - GEIMM
IGF040/93 (skin, fibroblast) - GEIMM
IGF040/94 (skin, fibroblast) - GEIMM
IGF040/95 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF040/96 (skin, fibroblast, adrenoleukodystrophy / addison disease and cerebral sclerosis) - GEIMM
IGF040/97 (skin, fibroblast, mannosidosis, alpha b, lysosomal) - GEIMM
IGF040/98 (skin, fibroblast) - GEIMM
IGF040/99 (skin, fibroblast) - GEIMM
IGF041/00 (skin, fibroblast) - GEIMM
IGF041/01 (skin, fibroblast) - GEIMM
IGF041/77 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF041/78 (skin, fibroblast) - GEIMM
IGF041/80 (skin, fibroblast, ichthyosis X-linked) - GEIMM
IGF041/81 (skin, fibroblast) - GEIMM
IGF041/84 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF041/85 (skin, fibroblast) - GEIMM
IGF041/86 (skin, fibroblast, hyperglycerolemia) - GEIMM
IGF041/87 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF041/88 (skin, fibroblast) - GEIMM
IGF041/89 (skin, fibroblast) - GEIMM
IGF041/90 (skin, fibroblast, geleophysic dwarfism) - GEIMM
IGF041/91 (skin, fibroblast) - GEIMM
IGF041/92 (skin, fibroblast) - GEIMM
IGF041/94 (skin, fibroblast, maple syrup urine disease) - GEIMM
IGF041/95 (skin, fibroblast, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF041/96 (skin, fibroblast) - GEIMM
IGF041/97 (skin, fibroblast) - GEIMM
IGF041/98 (skin, fibroblast) - GEIMM
IGF041/99 (skin, fibroblast) - GEIMM
IGF042/00 (skin, fibroblast) - GEIMM
IGF042/01 (skin, fibroblast) - GEIMM
IGF042/77 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF042/80 (skin, fibroblast) - GEIMM
IGF042/81 (skin, fibroblast) - GEIMM
IGF042/82 (skin, fibroblast) - GEIMM
IGF042/83 (skin, fibroblast) - GEIMM
IGF042/84 (skin, fibroblast) - GEIMM
IGF042/85 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF042/86 (skin, fibroblast) - GEIMM
IGF042/87 (skin, fibroblast) - GEIMM
IGF042/88 (skin, fibroblast) - GEIMM
IGF042/89 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF042/90 (skin, fibroblast, encephalopathy) - GEIMM
IGF042/91 (skin, fibroblast) - GEIMM
IGF042/92 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF042/93 (skin, fibroblast, Gaucher disease type II) - GEIMM
IGF042/94 (skin, fibroblast, Krabbe disease) - GEIMM
IGF042/95 (skin, fibroblast) - GEIMM
IGF042/96 (skin, fibroblast) - GEIMM
IGF042/97 (skin, fibroblast) - GEIMM
IGF042/98 (skin, fibroblast) - GEIMM
IGF042/99 (skin, fibroblast) - GEIMM
IGF043/00 (skin, fibroblast) - GEIMM
IGF043/77 (skin, fibroblast) - GEIMM
IGF043/78 (skin, fibroblast, ichthyosis X-linked) - GEIMM
IGF043/79 (skin, fibroblast) - GEIMM
IGF043/80 (skin, fibroblast) - GEIMM
IGF043/81 (skin, fibroblast) - GEIMM
IGF043/82 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF043/84 (skin, fibroblast) - GEIMM
IGF043/85 (skin, fibroblast) - GEIMM
IGF043/86 (skin, fibroblast) - GEIMM
IGF043/88 (skin, fibroblast) - GEIMM
IGF043/89 (skin, fibroblast) - GEIMM
IGF043/90 (skin, fibroblast) - GEIMM
IGF043/91 (skin, fibroblast, arsa pseudodeficiency) - GEIMM
IGF043/92 (skin, fibroblast) - GEIMM
IGF043/93 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF043/94 (skin, fibroblast) - GEIMM
IGF043/96 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGF043/97 (skin, fibroblast) - GEIMM
IGF043/98 (skin, fibroblast) - GEIMM
IGF043/99 (skin, fibroblast) - GEIMM
IGF044/00 (skin, fibroblast) - GEIMM
IGF044/77 (skin, fibroblast) - GEIMM
IGF044/78 (skin, fibroblast) - GEIMM
IGF044/79 (skin, fibroblast) - GEIMM
IGF044/81 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF044/82 (skin, fibroblast) - GEIMM
IGF044/83 (skin, fibroblast, adrenoleukodystrophy / addison disease and cerebral sclerosis) - GEIMM
IGF044/84 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF044/85 (skin, fibroblast) - GEIMM
IGF044/86 (skin, fibroblast, Marfan syndrome) - GEIMM
IGF044/87 (skin, fibroblast) - GEIMM
IGF044/88 (skin, fibroblast) - GEIMM
IGF044/89 (skin, fibroblast) - GEIMM
IGF044/90 (skin, fibroblast) - GEIMM
IGF044/91 (skin, fibroblast) - GEIMM
IGF044/92 (skin, fibroblast) - GEIMM
IGF044/93 (skin, fibroblast) - GEIMM
IGF044/94 (skin, fibroblast) - GEIMM
IGF044/95 (skin, fibroblast, Gaucher disease type II) - GEIMM
IGF044/96 (skin, fibroblast) - GEIMM
IGF044/97 (skin, fibroblast) - GEIMM
IGF044/98 (skin, fibroblast) - GEIMM
IGF044/99 (skin, fibroblast) - GEIMM
IGF045/00 (skin, fibroblast) - GEIMM
IGF045/78 (skin, fibroblast) - GEIMM
IGF045/79 (skin, fibroblast, mucolipidosis III) - GEIMM
IGF045/80 (skin, fibroblast) - GEIMM
IGF045/81 (skin, fibroblast) - GEIMM
IGF045/82 (skin, fibroblast) - GEIMM
IGF045/83 (skin, fibroblast) - GEIMM
IGF045/84 (skin, fibroblast) - GEIMM
IGF045/85 (skin, fibroblast) - GEIMM
IGF045/86 (skin, fibroblast) - GEIMM
IGF045/87 (skin, fibroblast) - GEIMM
IGF045/88 (skin, fibroblast) - GEIMM
IGF045/89 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF045/90 (skin, fibroblast, osteogenesis imperfecta, type II) - GEIMM
IGF045/91 (skin, fibroblast) - GEIMM
IGF045/92 (skin, fibroblast) - GEIMM
IGF045/93 (skin, fibroblast) - GEIMM
IGF045/94 (skin, fibroblast) - GEIMM
IGF045/95 (skin, fibroblast) - GEIMM
IGF045/96 (skin, fibroblast) - GEIMM
IGF045/97 (skin, fibroblast) - GEIMM
IGF045/98 (skin, fibroblast) - GEIMM
IGF045/99 (skin, fibroblast) - GEIMM
IGF046/00 (skin, fibroblast) - GEIMM
IGF046/76 (skin, fibroblast) - GEIMM
IGF046/78 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF046/79 (skin, fibroblast) - GEIMM
IGF046/80 (skin, fibroblast) - GEIMM
IGF046/82 (skin, fibroblast, Coffin-Lowry syndrome) - GEIMM
IGF046/83 (skin, fibroblast) - GEIMM
IGF046/84 (skin, fibroblast) - GEIMM
IGF046/85 (skin, fibroblast) - GEIMM
IGF046/87 (skin, fibroblast) - GEIMM
IGF046/89 (skin, fibroblast, osteogenesis imperfecta, type II) - GEIMM
IGF046/90 (skin, fibroblast, Krabbe disease) - GEIMM
IGF046/91 (skin, fibroblast) - GEIMM
IGF046/92 (skin, fibroblast, dystrophy congenital progressive) - GEIMM
IGF046/93 (skin, fibroblast) - GEIMM
IGF046/94 (skin, fibroblast) - GEIMM
IGF046/95 (skin, fibroblast, Costello syndrome) - GEIMM
IGF046/96 (skin, fibroblast) - GEIMM
IGF046/97 (skin, fibroblast) - GEIMM
IGF046/98 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF046/99 (skin, fibroblast) - GEIMM
IGF047/00 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF047/78 (skin, fibroblast, Gaucher disease type III) - GEIMM
IGF047/80 (skin, fibroblast) - GEIMM
IGF047/82 (skin, fibroblast, phenylketonuria II) - GEIMM
IGF047/83 (skin, fibroblast) - GEIMM
IGF047/84 (skin, fibroblast) - GEIMM
IGF047/85 (skin, fibroblast) - GEIMM
IGF047/86 (skin, fibroblast) - GEIMM
IGF047/87 (skin, fibroblast) - GEIMM
IGF047/88 (skin, fibroblast) - GEIMM
IGF047/89 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF047/90 (skin, fibroblast) - GEIMM
IGF047/91 (skin, fibroblast) - GEIMM
IGF047/92 (skin, fibroblast, osteogenesis imperfecta, type II) - GEIMM
IGF047/94 (skin, fibroblast) - GEIMM
IGF047/95 (skin, fibroblast, mucopolysaccharidosis type VI) - GEIMM
IGF047/96 (skin, fibroblast, maple syrup urine disease) - GEIMM
IGF047/97 (skin, fibroblast) - GEIMM
IGF047/98 (skin, fibroblast, amaurotic family idiocy, late infantile type/NCL late infantile) - GEIMM
IGF047/99 (skin, fibroblast) - GEIMM
IGF048/77 (skin, fibroblast) - GEIMM
IGF048/79 (skin, fibroblast) - GEIMM
IGF048/80 (skin, fibroblast, aspartylglycosaminuria) - GEIMM
IGF048/82 (skin, fibroblast, galactosemia) - GEIMM
IGF048/83 (skin, fibroblast) - GEIMM
IGF048/84 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF048/85 (skin, fibroblast) - GEIMM
IGF048/86 (skin, fibroblast, Niemann-Pick disease, type B) - GEIMM
IGF048/89 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF048/90 (skin, fibroblast) - GEIMM
IGF048/91 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF048/94 (skin, fibroblast, Marfan syndrome) - GEIMM
IGF048/95 (skin, fibroblast) - GEIMM
IGF048/96 (skin, fibroblast, muscolar dystrophy def.sarcoglican) - GEIMM
IGF048/97 (skin, fibroblast) - GEIMM
IGF048/98 (skin, fibroblast) - GEIMM
IGF048/99 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF049/00 (skin, fibroblast) - GEIMM
IGF049/77 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF049/78 (skin, fibroblast) - GEIMM
IGF049/79 (skin, fibroblast, Gaucher disease type III) - GEIMM
IGF049/80 (skin, fibroblast) - GEIMM
IGF049/82 (skin, fibroblast) - GEIMM
IGF049/83 (skin, fibroblast) - GEIMM
IGF049/84 (skin, fibroblast) - GEIMM
IGF049/85 (skin, fibroblast) - GEIMM
IGF049/86 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF049/87 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF049/89 (skin, fibroblast, homocystinuria) - GEIMM
IGF049/90 (skin, fibroblast, spinal muscolar atrophy I / Werdnig-Hoffmann disease) - GEIMM
IGF049/91 (skin, fibroblast, hypercholesterolemia, familial) - GEIMM
IGF049/92 (skin, fibroblast) - GEIMM
IGF049/93 (skin, fibroblast, Krabbe disease) - GEIMM
IGF049/94 (skin, fibroblast) - GEIMM
IGF049/95 (skin, fibroblast, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF049/96 (skin, fibroblast, SCID (severe combined immunodeficiency 1)) - GEIMM
IGF049/97 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF049/98 (skin, fibroblast) - GEIMM
IGF049/99 (skin, fibroblast, methylenetetra-hydrofolate reductase def.) - GEIMM
IGF050/00 (skin, fibroblast, Costello syndrome) - GEIMM
IGF050/76 (skin, fibroblast, fructose intolerance, hereditary) - GEIMM
IGF050/77 (skin, fibroblast) - GEIMM
IGF050/78 (skin, fibroblast) - GEIMM
IGF050/80 (skin, fibroblast) - GEIMM
IGF050/83 (skin, fibroblast) - GEIMM
IGF050/84 (skin, fibroblast) - GEIMM
IGF050/85 (skin, fibroblast) - GEIMM
IGF050/86 (skin, fibroblast, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF050/87 (skin, fibroblast) - GEIMM
IGF050/90 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF050/91 (skin, fibroblast) - GEIMM
IGF050/92 (skin, fibroblast, Aicardi syndrome / corpus callosum) - GEIMM
IGF050/93 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF050/97 (skin, fibroblast) - GEIMM
IGF050/98 (skin, fibroblast) - GEIMM
IGF050/99 (skin, fibroblast) - GEIMM
IGF051/00 (skin, fibroblast) - GEIMM
IGF051/77 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF051/78 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF051/80 (skin, fibroblast) - GEIMM
IGF051/82 (skin, fibroblast, angiokeratoma, diffuse / Fabry disease) - GEIMM
IGF051/83 (skin, fibroblast) - GEIMM
IGF051/84 (skin, fibroblast) - GEIMM
IGF051/85 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - GEIMM
IGF051/86 (skin, fibroblast) - GEIMM
IGF051/87 (skin, fibroblast) - GEIMM
IGF051/88 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF051/89 (skin, fibroblast) - GEIMM
IGF051/90 (skin, fibroblast) - GEIMM
IGF051/91 (skin, fibroblast, dibasicaminoaciduria II) - GEIMM
IGF051/92 (skin, fibroblast, mucopolysaccharidosis type VI) - GEIMM
IGF051/93 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF051/94 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF051/95 (skin, fibroblast) - GEIMM
IGF051/97 (skin, fibroblast, pycnodysostosis) - GEIMM
IGF051/98 (skin, fibroblast) - GEIMM
IGF051/99 (skin, fibroblast) - GEIMM
IGF052/00 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF052/76 (skin, fibroblast) - GEIMM
IGF052/77 (skin, fibroblast) - GEIMM
IGF052/78 (skin, fibroblast) - GEIMM
IGF052/80 (skin, fibroblast) - GEIMM
IGF052/81 (skin, fibroblast) - GEIMM
IGF052/82 (skin, fibroblast) - GEIMM
IGF052/83 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF052/84 (skin, fibroblast) - GEIMM
IGF052/85 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - GEIMM
IGF052/86 (skin, fibroblast, ataxia telangiectasia) - GEIMM
IGF052/87 (skin, fibroblast) - GEIMM
IGF052/88 (skin, fibroblast) - GEIMM
IGF052/89 (skin, fibroblast, hemochromatosis neonatal) - GEIMM
IGF052/90 (skin, fibroblast) - GEIMM
IGF052/91 (skin, fibroblast) - GEIMM
IGF052/92 (skin, fibroblast) - GEIMM
IGF052/93 (skin, fibroblast, Costello syndrome) - GEIMM
IGF052/94 (skin, fibroblast) - GEIMM
IGF052/95 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF052/97 (skin, fibroblast) - GEIMM
IGF052/99 (skin, fibroblast) - GEIMM
IGF053/00 (skin, fibroblast) - GEIMM
IGF053/78 (skin, fibroblast) - GEIMM
IGF053/80 (skin, fibroblast) - GEIMM
IGF053/81 (skin, fibroblast) - GEIMM
IGF053/83 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF053/84 (skin, fibroblast) - GEIMM
IGF053/85 (skin, fibroblast) - GEIMM
IGF053/86 (skin, fibroblast) - GEIMM
IGF053/87 (skin, fibroblast) - GEIMM
IGF053/89 (skin, fibroblast) - GEIMM
IGF053/90 (skin, fibroblast) - GEIMM
IGF053/91 (skin, fibroblast) - GEIMM
IGF053/92 (skin, fibroblast) - GEIMM
IGF053/94 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF053/97 (skin, fibroblast) - GEIMM
IGF053/99 (skin, fibroblast) - GEIMM
IGF054/77 (skin, fibroblast, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF054/78 (skin, fibroblast) - GEIMM
IGF054/80 (skin, fibroblast) - GEIMM
IGF054/82 (skin, fibroblast) - GEIMM
IGF054/83 (skin, fibroblast) - GEIMM
IGF054/84 (skin, fibroblast) - GEIMM
IGF054/85 (skin, fibroblast) - GEIMM
IGF054/86 (skin, fibroblast) - GEIMM
IGF054/89 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF054/90 (skin, fibroblast) - GEIMM
IGF054/91 (skin, fibroblast, dibasicaminoaciduria II) - GEIMM
IGF054/92 (skin, fibroblast, glycogen storage disease III) - GEIMM
IGF054/93 (skin, fibroblast, fucosidosis) - GEIMM
IGF054/94 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF054/95 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF054/97 (skin, fibroblast, pycnodysostosis) - GEIMM
IGF054/99 (skin, fibroblast) - GEIMM
IGF055/77 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF055/78 (skin, fibroblast) - GEIMM
IGF055/80 (skin, fibroblast) - GEIMM
IGF055/83 (skin, fibroblast) - GEIMM
IGF055/84 (skin, fibroblast) - GEIMM
IGF055/86 (skin, fibroblast) - GEIMM
IGF055/87 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF055/88 (skin, fibroblast, factor XIII deficiency) - GEIMM
IGF055/89 (skin, fibroblast, trisomy 21 / Down syndrome) - GEIMM
IGF055/90 (skin, fibroblast) - GEIMM
IGF055/92 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF055/93 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF055/94 (skin, fibroblast) - GEIMM
IGF055/95 (skin, fibroblast) - GEIMM
IGF055/97 (skin, fibroblast, neuraminidase deficiency) - GEIMM
IGF055/99 (skin, fibroblast) - GEIMM
IGF056/78 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGF056/79 (skin, fibroblast, cystic fibrosis) - GEIMM
IGF056/80 (skin, fibroblast) - GEIMM
IGF056/81 (skin, fibroblast, glycogen storage disease III) - GEIMM
IGF056/82 (skin, fibroblast) - GEIMM
IGF056/83 (skin, fibroblast) - GEIMM
IGF056/85 (skin, fibroblast) - GEIMM
IGF056/87 (skin, fibroblast, amaurotic family idiocy, late infantile type/NCL late infantile) - GEIMM
IGF056/90 (skin, fibroblast) - GEIMM
IGF056/91 (skin, fibroblast, chondrodysplasia punctata) - GEIMM
IGF056/92 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF056/93 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF056/94 (skin, fibroblast) - GEIMM
IGF056/95 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF056/97 (skin, fibroblast) - GEIMM
IGF057/76 (skin, fibroblast) - GEIMM
IGF057/77 (skin, fibroblast) - GEIMM
IGF057/78 (skin, fibroblast) - GEIMM
IGF057/80 (skin, fibroblast) - GEIMM
IGF057/81 (skin, fibroblast) - GEIMM
IGF057/82 (skin, fibroblast) - GEIMM
IGF057/83 (skin, fibroblast) - GEIMM
IGF057/84 (skin, fibroblast) - GEIMM
IGF057/85 (skin, fibroblast) - GEIMM
IGF057/86 (skin, fibroblast) - GEIMM
IGF057/87 (skin, fibroblast) - GEIMM
IGF057/88 (skin, fibroblast) - GEIMM
IGF057/89 (skin, fibroblast) - GEIMM
IGF057/90 (skin, fibroblast) - GEIMM
IGF057/91 (skin, fibroblast, Ehlers-Danlos syndrome, type I) - GEIMM
IGF057/92 (skin, fibroblast, Zellweger syndrome) - GEIMM
IGF057/93 (skin, fibroblast) - GEIMM
IGF057/95 (skin, fibroblast) - GEIMM
IGF057/97 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF058/78 (skin, fibroblast) - GEIMM
IGF058/79 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF058/80 (skin, fibroblast) - GEIMM
IGF058/82 (skin, fibroblast) - GEIMM
IGF058/83 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF058/84 (skin, fibroblast) - GEIMM
IGF058/85 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF058/86 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF058/87 (skin, fibroblast) - GEIMM
IGF058/89 (skin, fibroblast) - GEIMM
IGF058/90 (skin, fibroblast, osteogenesis imperfecta) - GEIMM
IGF058/91 (skin, fibroblast) - GEIMM
IGF058/93 (skin, fibroblast) - GEIMM
IGF058/95 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF058/97 (skin, fibroblast) - GEIMM
IGF059/76 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF059/78 (skin, fibroblast) - GEIMM
IGF059/79 (skin, fibroblast, gangliosidosis, generalized GM1, type II) - GEIMM
IGF059/80 (skin, fibroblast, Fanconi anemia, type I) - GEIMM
IGF059/82 (skin, fibroblast, Wolman disease/cholesterol ester storage disease) - GEIMM
IGF059/83 (skin, fibroblast) - GEIMM
IGF059/84 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF059/85 (skin, fibroblast) - GEIMM
IGF059/86 (skin, fibroblast) - GEIMM
IGF059/87 (skin, fibroblast) - GEIMM
IGF059/89 (skin, fibroblast) - GEIMM
IGF059/90 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF059/91 (skin, fibroblast) - GEIMM
IGF059/92 (skin, fibroblast) - GEIMM
IGF059/93 (skin, fibroblast) - GEIMM
IGF059/95 (skin, fibroblast) - GEIMM
IGF059/97 (skin, fibroblast) - GEIMM
IGF060/78 (skin, fibroblast, proteolipid protein, myelin) - GEIMM
IGF060/79 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF060/80 (skin, fibroblast) - GEIMM
IGF060/81 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF060/82 (skin, fibroblast, fibromatosis, juvenile hyaline) - GEIMM
IGF060/83 (skin, fibroblast) - GEIMM
IGF060/84 (skin, fibroblast, hyperglycinemia, nonketotic) - GEIMM
IGF060/86 (skin, fibroblast, osteogenesis imperfecta) - GEIMM
IGF060/87 (skin, fibroblast) - GEIMM
IGF060/88 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF060/89 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF060/90 (skin, fibroblast) - GEIMM
IGF060/91 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF060/92 (skin, fibroblast) - GEIMM
IGF060/93 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF060/95 (skin, fibroblast, homocystinuria - megaloblastic anemia) - GEIMM
IGF060/97 (skin, fibroblast, Krabbe disease) - GEIMM
IGF061/76 (skin, fibroblast) - GEIMM
IGF061/78 (skin, fibroblast) - GEIMM
IGF061/79 (skin, fibroblast, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF061/81 (skin, fibroblast, Hallervorden-Spatz disease) - GEIMM
IGF061/82 (skin, fibroblast) - GEIMM
IGF061/83 (skin, fibroblast) - GEIMM
IGF061/84 (skin, fibroblast) - GEIMM
IGF061/85 (skin, fibroblast, propionicacidemia I) - GEIMM
IGF061/86 (skin, fibroblast) - GEIMM
IGF061/87 (skin, fibroblast) - GEIMM
IGF061/88 (skin, fibroblast) - GEIMM
IGF061/89 (skin, fibroblast) - GEIMM
IGF061/90 (skin, fibroblast) - GEIMM
IGF061/91 (skin, fibroblast) - GEIMM
IGF061/92 (skin, fibroblast) - GEIMM
IGF061/93 (skin, fibroblast) - GEIMM
IGF061/95 (skin, fibroblast, Wolman disease/cholesterol ester storage disease) - GEIMM
IGF061/97 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF062/78 (skin, fibroblast) - GEIMM
IGF062/79 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF062/81 (skin, fibroblast) - GEIMM
IGF062/82 (skin, fibroblast) - GEIMM
IGF062/83 (skin, fibroblast) - GEIMM
IGF062/84 (skin, fibroblast) - GEIMM
IGF062/85 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF062/86 (skin, fibroblast, osteogenesis imperfecta, type II) - GEIMM
IGF062/87 (skin, fibroblast) - GEIMM
IGF062/88 (skin, fibroblast) - GEIMM
IGF062/89 (skin, fibroblast, neuraminidase deficiency with beta-galactosidase deficiency) - GEIMM
IGF062/90 (skin, fibroblast, Costello syndrome) - GEIMM
IGF062/91 (skin, fibroblast) - GEIMM
IGF062/95 (skin, fibroblast, Glutaricacidemia I) - GEIMM
IGF062/97 (skin, fibroblast) - GEIMM
IGF063/76 (skin, fibroblast) - GEIMM
IGF063/77 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF063/78 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF063/79 (skin, fibroblast) - GEIMM
IGF063/80 (skin, fibroblast) - GEIMM
IGF063/81 (skin, fibroblast) - GEIMM
IGF063/82 (skin, fibroblast) - GEIMM
IGF063/84 (skin, fibroblast) - GEIMM
IGF063/85 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF063/86 (skin, fibroblast, mucopolysaccharidosis type III B) - GEIMM
IGF063/87 (skin, fibroblast) - GEIMM
IGF063/90 (skin, fibroblast) - GEIMM
IGF063/91 (skin, fibroblast) - GEIMM
IGF063/93 (skin, fibroblast) - GEIMM
IGF063/95 (skin, fibroblast, homocystinuria - megaloblastic anemia) - GEIMM
IGF063/96 (skin, fibroblast) - GEIMM
IGF064/76 (skin, fibroblast) - GEIMM
IGF064/78 (skin, fibroblast) - GEIMM
IGF064/79 (skin, fibroblast) - GEIMM
IGF064/80 (skin, fibroblast) - GEIMM
IGF064/81 (skin, fibroblast, Wilson disease) - GEIMM
IGF064/82 (skin, fibroblast) - GEIMM
IGF064/83 (skin, fibroblast) - GEIMM
IGF064/84 (skin, fibroblast) - GEIMM
IGF064/85 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF064/86 (skin, fibroblast, mucopolysaccharidosis type III B) - GEIMM
IGF064/87 (skin, fibroblast) - GEIMM
IGF064/88 (skin, fibroblast) - GEIMM
IGF064/89 (skin, fibroblast) - GEIMM
IGF064/90 (skin, fibroblast) - GEIMM
IGF064/91 (skin, fibroblast) - GEIMM
IGF064/93 (skin, fibroblast) - GEIMM
IGF064/95 (skin, fibroblast) - GEIMM
IGF065/77 (skin, fibroblast) - GEIMM
IGF065/79 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF065/80 (skin, fibroblast) - GEIMM
IGF065/81 (skin, fibroblast) - GEIMM
IGF065/83 (skin, fibroblast) - GEIMM
IGF065/84 (skin, fibroblast) - GEIMM
IGF065/86 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF065/87 (skin, fibroblast) - GEIMM
IGF065/88 (skin, fibroblast, osteogenesis imperfecta) - GEIMM
IGF065/90 (skin, fibroblast, testicular feminization syndrome) - GEIMM
IGF065/91 (skin, fibroblast, Ehlers-Danlos syndrome) - GEIMM
IGF065/92 (skin, fibroblast, Sjogren-Larsson syndrome) - GEIMM
IGF065/93 (skin, fibroblast, mitochondrial respiratory chain complex I) - GEIMM
IGF065/95 (skin, fibroblast) - GEIMM
IGF066/76 (skin, fibroblast) - GEIMM
IGF066/77 (skin, fibroblast) - GEIMM
IGF066/78 (skin, fibroblast) - GEIMM
IGF066/79 (skin, fibroblast) - GEIMM
IGF066/80 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF066/82 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF066/83 (skin, fibroblast) - GEIMM
IGF066/84 (skin, fibroblast, homocystinuria) - GEIMM
IGF066/85 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF066/86 (skin, fibroblast) - GEIMM
IGF066/87 (skin, fibroblast, mucopolysaccharidosis type III B) - GEIMM
IGF066/88 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF066/89 (skin, fibroblast) - GEIMM
IGF066/90 (skin, fibroblast, spinal muscolar atrophy I / Werdnig-Hoffmann disease) - GEIMM
IGF066/91 (skin, fibroblast, carboydrate deficient glycoprotein syndrome, type I) - GEIMM
IGF066/92 (skin, fibroblast) - GEIMM
IGF066/93 (skin, fibroblast) - GEIMM
IGF066/95 (skin, fibroblast) - GEIMM
IGF067/78 (skin, fibroblast) - GEIMM
IGF067/81 (skin, fibroblast) - GEIMM
IGF067/82 (skin, fibroblast, methylmalonicacidemia) - GEIMM
IGF067/83 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF067/84 (skin, fibroblast, arsa pseudodeficiency) - GEIMM
IGF067/85 (skin, fibroblast) - GEIMM
IGF067/86 (skin, fibroblast) - GEIMM
IGF067/87 (skin, fibroblast, arthrogryposis multiplex congenita) - GEIMM
IGF067/88 (skin, fibroblast) - GEIMM
IGF067/89 (skin, fibroblast) - GEIMM
IGF067/90 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF067/91 (skin, fibroblast, Zellweger syndrome) - GEIMM
IGF067/92 (skin, fibroblast) - GEIMM
IGF067/93 (skin, fibroblast) - GEIMM
IGF067/95 (skin, fibroblast) - GEIMM
IGF068/78 (skin, fibroblast) - GEIMM
IGF068/79 (skin, fibroblast, cystic fibrosis) - GEIMM
IGF068/80 (skin, fibroblast) - GEIMM
IGF068/82 (skin, fibroblast, Aldrich syndrome) - GEIMM
IGF068/83 (skin, fibroblast, Niemann-Pick disease, type B) - GEIMM
IGF068/84 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF068/85 (skin, fibroblast) - GEIMM
IGF068/86 (skin, fibroblast) - GEIMM
IGF068/87 (skin, fibroblast) - GEIMM
IGF068/88 (skin, fibroblast) - GEIMM
IGF068/89 (skin, fibroblast, post-traumatic osteoporosis) - GEIMM
IGF068/90 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF068/91 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF068/92 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF068/93 (skin, fibroblast) - GEIMM
IGF068/95 (skin, fibroblast) - GEIMM
IGF069/78 (skin, fibroblast) - GEIMM
IGF069/80 (skin, fibroblast) - GEIMM
IGF069/82 (skin, fibroblast) - GEIMM
IGF069/84 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF069/85 (skin, fibroblast) - GEIMM
IGF069/86 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF069/87 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF069/88 (skin, fibroblast) - GEIMM
IGF069/89 (skin, fibroblast) - GEIMM
IGF069/90 (skin, fibroblast) - GEIMM
IGF069/91 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF069/92 (skin, fibroblast) - GEIMM
IGF069/93 (skin, fibroblast) - GEIMM
IGF069/95 (skin, fibroblast) - GEIMM
IGF070/76 (skin, fibroblast) - GEIMM
IGF070/78 (skin, fibroblast) - GEIMM
IGF070/80 (skin, fibroblast) - GEIMM
IGF070/81 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF070/82 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGF070/83 (skin, fibroblast, Gaucher disease type III) - GEIMM
IGF070/84 (skin, fibroblast) - GEIMM
IGF070/85 (skin, fibroblast) - GEIMM
IGF070/86 (skin, fibroblast, adrenoleukodystrophy / addison disease and cerebral sclerosis) - GEIMM
IGF070/87 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF070/88 (skin, fibroblast, pyruvate dehydrogenase def.) - GEIMM
IGF070/89 (skin, fibroblast, Edwards' syndrome / trisomy 18) - GEIMM
IGF070/90 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF070/91 (skin, fibroblast) - GEIMM
IGF070/92 (skin, fibroblast) - GEIMM
IGF070/93 (skin, fibroblast) - GEIMM
IGF070/95 (skin, fibroblast) - GEIMM
IGF071/76 (skin, fibroblast) - GEIMM
IGF071/78 (skin, fibroblast, Turner syndrome/noonan syndrome 1) - GEIMM
IGF071/80 (skin, fibroblast) - GEIMM
IGF071/81 (skin, fibroblast) - GEIMM
IGF071/82 (skin, fibroblast) - GEIMM
IGF071/83 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF071/84 (skin, fibroblast) - GEIMM
IGF071/85 (skin, fibroblast, spinal muscolar atrophy I / Werdnig-Hoffmann disease) - GEIMM
IGF071/86 (skin, fibroblast) - GEIMM
IGF071/87 (skin, fibroblast) - GEIMM
IGF071/88 (skin, fibroblast) - GEIMM
IGF071/89 (skin, fibroblast, spinal muscolar atrophy I / Werdnig-Hoffmann disease) - GEIMM
IGF071/90 (skin, fibroblast) - GEIMM
IGF071/92 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF071/93 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF071/95 (skin, fibroblast, metachromatic leukodystrophy) - GEIMM
IGF072/76 (skin, fibroblast) - GEIMM
IGF072/77 (skin, fibroblast) - GEIMM
IGF072/78 (skin, fibroblast) - GEIMM
IGF072/81 (skin, fibroblast) - GEIMM
IGF072/82 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF072/83 (skin, fibroblast, homocystinuria) - GEIMM
IGF072/84 (skin, fibroblast) - GEIMM
IGF072/85 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF072/86 (skin, fibroblast) - GEIMM
IGF072/87 (skin, fibroblast) - GEIMM
IGF072/88 (skin, fibroblast) - GEIMM
IGF072/89 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF072/90 (skin, fibroblast) - GEIMM
IGF072/91 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF072/92 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF072/95 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF073/76 (skin, fibroblast) - GEIMM
IGF073/78 (skin, fibroblast) - GEIMM
IGF073/82 (skin, fibroblast) - GEIMM
IGF073/83 (skin, fibroblast) - GEIMM
IGF073/84 (skin, fibroblast) - GEIMM
IGF073/85 (skin, fibroblast, Turner syndrome/noonan syndrome 1) - GEIMM
IGF073/86 (skin, fibroblast) - GEIMM
IGF073/87 (skin, fibroblast) - GEIMM
IGF073/88 (skin, fibroblast) - GEIMM
IGF073/89 (skin, fibroblast) - GEIMM
IGF073/90 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF073/91 (skin, fibroblast, geroderma osteodysplastica) - GEIMM
IGF073/92 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF073/95 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF074/76 (skin, fibroblast, triglyceride storage disease) - GEIMM
IGF074/78 (skin, fibroblast, Laurence-Moon syndrome) - GEIMM
IGF074/79 (skin, fibroblast) - GEIMM
IGF074/81 (skin, fibroblast) - GEIMM
IGF074/82 (skin, fibroblast) - GEIMM
IGF074/83 (skin, fibroblast) - GEIMM
IGF074/84 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF074/86 (skin, fibroblast) - GEIMM
IGF074/87 (skin, fibroblast) - GEIMM
IGF074/88 (skin, fibroblast) - GEIMM
IGF074/89 (skin, fibroblast, Ellis-Van Creveld syndrome) - GEIMM
IGF074/90 (skin, fibroblast) - GEIMM
IGF074/92 (skin, fibroblast, Cockayne syndrome) - GEIMM
IGF075/76 (skin, fibroblast) - GEIMM
IGF075/77 (skin, fibroblast) - GEIMM
IGF075/78 (skin, fibroblast, aspartylglycosaminuria) - GEIMM
IGF075/80 (skin, fibroblast, sulfatidosis, juvenile, Austin type) - GEIMM
IGF075/81 (skin, fibroblast, Krabbe disease) - GEIMM
IGF075/82 (skin, fibroblast, mucopolysaccharidosis type III C) - GEIMM
IGF075/84 (skin, fibroblast) - GEIMM
IGF075/86 (skin, fibroblast, amaurotic family idiocy, late infantile type/NCL late infantile) - GEIMM
IGF075/87 (skin, fibroblast) - GEIMM
IGF075/88 (skin, fibroblast) - GEIMM
IGF075/89 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF075/90 (skin, fibroblast) - GEIMM
IGF075/91 (skin, fibroblast) - GEIMM
IGF075/95 (skin, fibroblast) - GEIMM
IGF076/76 (skin, fibroblast) - GEIMM
IGF076/78 (skin, fibroblast) - GEIMM
IGF076/79 (skin, fibroblast) - GEIMM
IGF076/81 (skin, fibroblast) - GEIMM
IGF076/82 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF076/83 (skin, fibroblast) - GEIMM
IGF076/84 (skin, fibroblast, dystonia musculorum deformans 2) - GEIMM
IGF076/85 (skin, fibroblast) - GEIMM
IGF076/87 (skin, fibroblast) - GEIMM
IGF076/89 (skin, fibroblast, Smith-McCort dwarfism) - GEIMM
IGF076/90 (skin, fibroblast) - GEIMM
IGF076/91 (skin, fibroblast, Menkes syndrome) - GEIMM
IGF076/92 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF076/95 (skin, fibroblast) - GEIMM
IGF077/76 (skin, fibroblast) - GEIMM
IGF077/77 (skin, fibroblast) - GEIMM
IGF077/78 (skin, fibroblast) - GEIMM
IGF077/79 (skin, fibroblast) - GEIMM
IGF077/80 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF077/81 (skin, fibroblast, Krabbe disease) - GEIMM
IGF077/83 (skin, fibroblast) - GEIMM
IGF077/84 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF077/85 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF077/86 (skin, fibroblast) - GEIMM
IGF077/87 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGF077/88 (skin, fibroblast, Sandhoff disease) - GEIMM
IGF077/89 (skin, fibroblast, mucolipidosis III) - GEIMM
IGF077/91 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF077/92 (skin, fibroblast, spinal muscolar atrophy I / Werdnig-Hoffmann disease) - GEIMM
IGF077/95 (skin, fibroblast) - GEIMM
IGF078/78 (skin, fibroblast) - GEIMM
IGF078/79 (skin, fibroblast) - GEIMM
IGF078/80 (skin, fibroblast) - GEIMM
IGF078/81 (skin, fibroblast) - GEIMM
IGF078/83 (skin, fibroblast) - GEIMM
IGF078/84 (skin, fibroblast, amaurotic family idiocy, late infantile type/NCL late infantile) - GEIMM
IGF078/85 (skin, fibroblast) - GEIMM
IGF078/86 (skin, fibroblast) - GEIMM
IGF078/87 (skin, fibroblast) - GEIMM
IGF078/89 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF078/90 (skin, fibroblast) - GEIMM
IGF078/91 (skin, fibroblast) - GEIMM
IGF078/92 (skin, fibroblast) - GEIMM
IGF078/95 (skin, fibroblast) - GEIMM
IGF079/76 (skin, fibroblast, Ehlers-Danlos syndrome) - GEIMM
IGF079/77 (skin, fibroblast) - GEIMM
IGF079/78 (skin, fibroblast, spondyloepiphyseal dysplasia, congenital) - GEIMM
IGF079/80 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF079/81 (skin, fibroblast) - GEIMM
IGF079/82 (skin, fibroblast) - GEIMM
IGF079/83 (skin, fibroblast) - GEIMM
IGF079/84 (skin, fibroblast) - GEIMM
IGF079/86 (skin, fibroblast) - GEIMM
IGF079/87 (skin, fibroblast) - GEIMM
IGF079/89 (skin, fibroblast, familial dolichocephaly) - GEIMM
IGF079/90 (skin, fibroblast, early myoclonic encephalopathy) - GEIMM
IGF079/91 (skin, fibroblast) - GEIMM
IGF080/76 (skin, fibroblast, mucolipidosis III) - GEIMM
IGF080/78 (skin, fibroblast) - GEIMM
IGF080/80 (skin, fibroblast) - GEIMM
IGF080/81 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGF080/82 (skin, fibroblast) - GEIMM
IGF080/83 (skin, fibroblast) - GEIMM
IGF080/84 (skin, fibroblast) - GEIMM
IGF080/85 (skin, fibroblast, glycogen storage disease III) - GEIMM
IGF080/86 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF080/87 (skin, fibroblast) - GEIMM
IGF080/89 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF080/90 (skin, fibroblast) - GEIMM
IGF080/91 (skin, fibroblast) - GEIMM
IGF081/76 (skin, fibroblast, mucolipidosis III) - GEIMM
IGF081/78 (skin, fibroblast, mannosidosis, alpha b, lysosomal) - GEIMM
IGF081/80 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF081/81 (skin, fibroblast, Menkes syndrome) - GEIMM
IGF081/82 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF081/83 (skin, fibroblast) - GEIMM
IGF081/84 (skin, fibroblast, mucopolysaccharidosis type III B) - GEIMM
IGF081/86 (skin, fibroblast, diastrophic dysplasia) - GEIMM
IGF081/87 (skin, fibroblast) - GEIMM
IGF081/89 (skin, fibroblast, sudden infant death syndrome) - GEIMM
IGF081/90 (skin, fibroblast, fucosidosis) - GEIMM
IGF081/91 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF081/92 (skin, fibroblast, Sjogren-Larsson syndrome) - GEIMM
IGF082/76 (skin, fibroblast, Farber lipogranulomatosis) - GEIMM
IGF082/80 (skin, fibroblast) - GEIMM
IGF082/81 (skin, fibroblast) - GEIMM
IGF082/82 (skin, fibroblast) - GEIMM
IGF082/83 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF082/84 (skin, fibroblast) - GEIMM
IGF082/85 (skin, fibroblast) - GEIMM
IGF082/86 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF082/87 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF082/89 (skin, fibroblast) - GEIMM
IGF082/90 (skin, fibroblast) - GEIMM
IGF082/91 (skin, fibroblast, mucopolysaccharidosis type III B) - GEIMM
IGF082/92 (skin, fibroblast) - GEIMM
IGF083/76 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF083/78 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF083/80 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF083/81 (skin, fibroblast) - GEIMM
IGF083/82 (skin, fibroblast, hyperglycinemia, nonketotic) - GEIMM
IGF083/83 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF083/84 (skin, fibroblast, angiokeratoma, diffuse / Fabry disease) - GEIMM
IGF083/85 (skin, fibroblast, spinal muscolar atrophy I / Werdnig-Hoffmann disease) - GEIMM
IGF083/86 (skin, fibroblast) - GEIMM
IGF083/87 (skin, fibroblast) - GEIMM
IGF083/89 (skin, fibroblast) - GEIMM
IGF083/90 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF083/91 (skin, fibroblast) - GEIMM
IGF083/92 (skin, fibroblast) - GEIMM
IGF084/80 (skin, fibroblast) - GEIMM
IGF084/81 (skin, fibroblast) - GEIMM
IGF084/82 (skin, fibroblast, gangliosidosis, generalized GM1, type II) - GEIMM
IGF084/83 (skin, fibroblast) - GEIMM
IGF084/84 (skin, fibroblast) - GEIMM
IGF084/85 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF084/86 (skin, fibroblast) - GEIMM
IGF084/89 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF084/90 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF084/91 (skin, fibroblast, proteolipid protein, myelin) - GEIMM
IGF084/92 (skin, fibroblast) - GEIMM
IGF085/78 (skin, fibroblast) - GEIMM
IGF085/80 (skin, fibroblast) - GEIMM
IGF085/82 (skin, fibroblast) - GEIMM
IGF085/84 (skin, fibroblast) - GEIMM
IGF085/85 (skin, fibroblast) - GEIMM
IGF085/86 (skin, fibroblast, complex IV,mitocondrial respiratory chain,deficiency of) - GEIMM
IGF085/89 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF085/90 (skin, fibroblast, Krabbe disease) - GEIMM
IGF085/91 (skin, fibroblast) - GEIMM
IGF085/92 (skin, fibroblast) - GEIMM
IGF086/78 (skin, fibroblast, Krabbe disease) - GEIMM
IGF086/79 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF086/80 (skin, fibroblast) - GEIMM
IGF086/84 (skin, fibroblast) - GEIMM
IGF086/85 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF086/86 (skin, fibroblast) - GEIMM
IGF086/89 (skin, fibroblast) - GEIMM
IGF086/90 (skin, fibroblast, Lesch-Nyhan syndrome) - GEIMM
IGF086/91 (skin, fibroblast, adrenoleukodystrophy / addison disease and cerebral sclerosis) - GEIMM
IGF086/92 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF087/78 (skin, fibroblast) - GEIMM
IGF087/79 (skin, fibroblast, amaurotic family idiocy, late infantile type/NCL late infantile) - GEIMM
IGF087/80 (skin, fibroblast) - GEIMM
IGF087/81 (skin, fibroblast) - GEIMM
IGF087/82 (skin, fibroblast) - GEIMM
IGF087/83 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF087/84 (skin, fibroblast) - GEIMM
IGF087/85 (skin, fibroblast) - GEIMM
IGF087/86 (skin, fibroblast) - GEIMM
IGF087/87 (skin, fibroblast) - GEIMM
IGF087/89 (skin, fibroblast) - GEIMM
IGF087/91 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF087/92 (skin, fibroblast, spongy degeneration of central nervous system /Canavan disease) - GEIMM
IGF088/78 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGF088/79 (skin, fibroblast) - GEIMM
IGF088/82 (skin, fibroblast) - GEIMM
IGF088/83 (skin, fibroblast) - GEIMM
IGF088/84 (skin, fibroblast) - GEIMM
IGF088/86 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGF088/87 (skin, fibroblast) - GEIMM
IGF088/89 (skin, fibroblast) - GEIMM
IGF088/90 (skin, fibroblast) - GEIMM
IGF088/91 (skin, fibroblast) - GEIMM
IGF088/92 (skin, fibroblast) - GEIMM
IGF089/78 (skin, fibroblast) - GEIMM
IGF089/79 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF089/80 (skin, fibroblast, B1 variant - GM2 gangliosidosis / Tay-Sachs disease) - GEIMM
IGF089/81 (skin, fibroblast) - GEIMM
IGF089/82 (skin, fibroblast, frontometaphyseal dysplasia) - GEIMM
IGF089/83 (skin, fibroblast, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF089/84 (skin, fibroblast) - GEIMM
IGF089/85 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF089/87 (skin, fibroblast, osteogenesis imperfecta, type II) - GEIMM
IGF089/89 (skin, fibroblast, osteogenesis imperfecta, type II) - GEIMM
IGF089/90 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF089/91 (skin, fibroblast) - GEIMM
IGF089/92 (skin, fibroblast) - GEIMM
IGF090/78 (skin, fibroblast, Laurence-Moon syndrome) - GEIMM
IGF090/79 (skin, fibroblast) - GEIMM
IGF090/82 (skin, fibroblast) - GEIMM
IGF090/83 (skin, fibroblast) - GEIMM
IGF090/84 (skin, fibroblast) - GEIMM
IGF090/86 (skin, fibroblast, Larsen syndrome) - GEIMM
IGF090/87 (skin, fibroblast, osteogenesis imperfecta) - GEIMM
IGF090/89 (skin, fibroblast) - GEIMM
IGF090/91 (skin, fibroblast, carboydrate deficient glycoprotein syndrome, type I) - GEIMM
IGF090/92 (skin, fibroblast) - GEIMM
IGF091/78 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF091/79 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF091/81 (skin, fibroblast) - GEIMM
IGF091/82 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF091/83 (skin, fibroblast) - GEIMM
IGF091/84 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF091/85 (skin, fibroblast, argininosuccinicaciduria) - GEIMM
IGF091/86 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF091/87 (skin, fibroblast) - GEIMM
IGF091/89 (skin, fibroblast) - GEIMM
IGF091/92 (skin, fibroblast) - GEIMM
IGF092/78 (skin, fibroblast) - GEIMM
IGF092/82 (skin, fibroblast, phenylketonuria I) - GEIMM
IGF092/83 (skin, fibroblast) - GEIMM
IGF092/84 (skin, fibroblast, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF092/86 (skin, fibroblast) - GEIMM
IGF092/87 (skin, fibroblast) - GEIMM
IGF093/78 (skin, fibroblast) - GEIMM
IGF093/80 (skin, fibroblast) - GEIMM
IGF093/81 (skin, fibroblast) - GEIMM
IGF093/82 (skin, fibroblast) - GEIMM
IGF093/83 (skin, fibroblast) - GEIMM
IGF093/84 (skin, fibroblast) - GEIMM
IGF093/85 (skin, fibroblast, osteogenesis imperfecta) - GEIMM
IGF093/86 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF093/87 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF093/89 (skin, fibroblast, osteogenesis imperfecta, type IV) - GEIMM
IGF093/90 (skin, fibroblast) - GEIMM
IGF093/91 (skin, fibroblast, Krabbe disease) - GEIMM
IGF093/92 (skin, fibroblast) - GEIMM
IGF094/78 (skin, fibroblast, arsa pseudodeficiency) - GEIMM
IGF094/80 (skin, fibroblast) - GEIMM
IGF094/81 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF094/83 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF094/84 (skin, fibroblast) - GEIMM
IGF094/85 (skin, fibroblast) - GEIMM
IGF094/86 (skin, fibroblast) - GEIMM
IGF094/87 (skin, fibroblast) - GEIMM
IGF094/89 (skin, fibroblast) - GEIMM
IGF094/90 (skin, fibroblast) - GEIMM
IGF094/91 (skin, fibroblast) - GEIMM
IGF094/92 (skin, fibroblast, homocystinuria - megaloblastic anemia) - GEIMM
IGF095/78 (skin, fibroblast) - GEIMM
IGF095/79 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF095/80 (skin, fibroblast) - GEIMM
IGF095/82 (skin, fibroblast) - GEIMM
IGF095/83 (skin, fibroblast) - GEIMM
IGF095/85 (skin, fibroblast, Shwachman-Bodian syndrome) - GEIMM
IGF095/86 (skin, fibroblast, Krabbe disease) - GEIMM
IGF095/87 (skin, fibroblast) - GEIMM
IGF095/89 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF095/91 (skin, fibroblast) - GEIMM
IGF096/78 (skin, fibroblast) - GEIMM
IGF096/79 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF096/80 (skin, fibroblast) - GEIMM
IGF096/81 (skin, fibroblast) - GEIMM
IGF096/82 (skin, fibroblast, Ehlers-Danlos syndrome) - GEIMM
IGF096/83 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF096/84 (skin, fibroblast, camptomelic dwarfism) - GEIMM
IGF096/85 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF096/86 (skin, fibroblast) - GEIMM
IGF096/90 (skin, fibroblast) - GEIMM
IGF096/91 (skin, fibroblast) - GEIMM
IGF096/92 (skin, fibroblast) - GEIMM
IGF097/78 (skin, fibroblast) - GEIMM
IGF097/79 (skin, fibroblast) - GEIMM
IGF097/80 (skin, fibroblast) - GEIMM
IGF097/81 (skin, fibroblast) - GEIMM
IGF097/82 (skin, fibroblast) - GEIMM
IGF097/83 (skin, fibroblast) - GEIMM
IGF097/84 (skin, fibroblast) - GEIMM
IGF097/85 (skin, fibroblast) - GEIMM
IGF097/86 (skin, fibroblast, Gaucher disease type III) - GEIMM
IGF097/87 (skin, fibroblast) - GEIMM
IGF097/89 (skin, fibroblast, cri du chat syndrome) - GEIMM
IGF097/90 (skin, fibroblast, spastic paraparesis) - GEIMM
IGF097/92 (skin, fibroblast) - GEIMM
IGF098/78 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF098/79 (skin, fibroblast) - GEIMM
IGF098/80 (skin, fibroblast) - GEIMM
IGF098/82 (skin, fibroblast) - GEIMM
IGF098/83 (skin, fibroblast) - GEIMM
IGF098/84 (skin, fibroblast) - GEIMM
IGF098/85 (skin, fibroblast) - GEIMM
IGF098/86 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF098/87 (skin, fibroblast) - GEIMM
IGF098/90 (skin, fibroblast) - GEIMM
IGF098/92 (skin, fibroblast, glyceronephosphate o-acyltransferase) - GEIMM
IGF099/78 (skin, fibroblast) - GEIMM
IGF099/79 (skin, fibroblast, adrenal hyperplasia III) - GEIMM
IGF099/80 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF099/82 (skin, fibroblast) - GEIMM
IGF099/83 (skin, fibroblast) - GEIMM
IGF099/84 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF099/85 (skin, fibroblast) - GEIMM
IGF099/86 (skin, fibroblast, fibrodysplasia ossificans progressiva) - GEIMM
IGF099/87 (skin, fibroblast) - GEIMM
IGF099/89 (skin, fibroblast) - GEIMM
IGF099/90 (skin, fibroblast, spinal muscolar atrophy III) - GEIMM
IGF099/92 (skin, fibroblast) - GEIMM
IGF100/78 (skin, fibroblast, mucopolysaccharidosis type VI) - GEIMM
IGF100/79 (skin, fibroblast) - GEIMM
IGF100/80 (skin, fibroblast) - GEIMM
IGF100/81 (skin, fibroblast, porphiria, acute intermittent) - GEIMM
IGF100/83 (skin, fibroblast) - GEIMM
IGF100/84 (skin, fibroblast) - GEIMM
IGF100/85 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF100/86 (skin, fibroblast) - GEIMM
IGF100/87 (skin, fibroblast) - GEIMM
IGF100/89 (skin, fibroblast, spinal muscolar atrophy I / Werdnig-Hoffmann disease) - GEIMM
IGF100/90 (skin, fibroblast, osteogenesis imperfecta) - GEIMM
IGF100/91 (skin, fibroblast, articular hypermobility syndrome) - GEIMM
IGF100/92 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF101/78 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF101/79 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF101/80 (skin, fibroblast, homocystinuria) - GEIMM
IGF101/81 (skin, fibroblast, trichothiodystrophy) - GEIMM
IGF101/82 (skin, fibroblast) - GEIMM
IGF101/83 (skin, fibroblast, mucopolysaccharidosis type III C) - GEIMM
IGF101/84 (skin, fibroblast) - GEIMM
IGF101/85 (skin, fibroblast) - GEIMM
IGF101/86 (skin, fibroblast) - GEIMM
IGF101/89 (skin, fibroblast) - GEIMM
IGF101/90 (skin, fibroblast) - GEIMM
IGF101/91 (skin, fibroblast, Marfan syndrome) - GEIMM
IGF102/78 (skin, fibroblast, neuraminidase deficiency) - GEIMM
IGF102/80 (skin, fibroblast, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF102/82 (skin, fibroblast) - GEIMM
IGF102/83 (skin, fibroblast, hyperlipoproteinemia I) - GEIMM
IGF102/84 (skin, fibroblast) - GEIMM
IGF102/85 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF102/86 (skin, fibroblast) - GEIMM
IGF102/87 (skin, fibroblast) - GEIMM
IGF102/89 (skin, fibroblast, trisomy 21 / Down syndrome) - GEIMM
IGF102/90 (skin, fibroblast) - GEIMM
IGF102/91 (skin, fibroblast, Marfan syndrome) - GEIMM
IGF103/79 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF103/81 (skin, fibroblast, propionicacidemia I) - GEIMM
IGF103/82 (skin, fibroblast) - GEIMM
IGF103/84 (skin, fibroblast) - GEIMM
IGF103/85 (skin, fibroblast) - GEIMM
IGF103/86 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF103/89 (skin, fibroblast) - GEIMM
IGF103/90 (skin, fibroblast) - GEIMM
IGF103/91 (skin, fibroblast, Marfan syndrome) - GEIMM
IGF104/78 (skin, fibroblast, gangliosidosis, generalized GM1, type II) - GEIMM
IGF104/79 (skin, fibroblast, mucopolysaccharidosis type III B) - GEIMM
IGF104/81 (skin, fibroblast, maple syrup urine disease) - GEIMM
IGF104/82 (skin, fibroblast, Lesch-Nyhan syndrome) - GEIMM
IGF104/83 (skin, fibroblast) - GEIMM
IGF104/84 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF104/85 (skin, fibroblast) - GEIMM
IGF104/89 (skin, fibroblast) - GEIMM
IGF104/90 (skin, fibroblast) - GEIMM
IGF104/91 (skin, fibroblast) - GEIMM
IGF105/80 (skin, fibroblast) - GEIMM
IGF105/81 (skin, fibroblast, fucosidosis) - GEIMM
IGF105/82 (skin, fibroblast) - GEIMM
IGF105/83 (skin, fibroblast) - GEIMM
IGF105/84 (skin, fibroblast) - GEIMM
IGF105/85 (skin, fibroblast, Lowe oculocerebrorenal syndrome) - GEIMM
IGF105/87 (skin, fibroblast) - GEIMM
IGF105/89 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGF105/91 (skin, fibroblast) - GEIMM
IGF106/78 (skin, fibroblast) - GEIMM
IGF106/79 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF106/80 (skin, fibroblast) - GEIMM
IGF106/81 (skin, fibroblast) - GEIMM
IGF106/82 (skin, fibroblast) - GEIMM
IGF106/83 (skin, fibroblast, mucopolysaccharidosis type III B) - GEIMM
IGF106/84 (skin, fibroblast) - GEIMM
IGF106/85 (skin, fibroblast) - GEIMM
IGF106/90 (skin, fibroblast) - GEIMM
IGF106/91 (skin, fibroblast, mucopolysaccharidosis type III C) - GEIMM
IGF107/80 (skin, fibroblast) - GEIMM
IGF107/81 (skin, fibroblast, fructose intolerance, hereditary) - GEIMM
IGF107/82 (skin, fibroblast, Bardet-Biedl syndrome) - GEIMM
IGF107/83 (skin, fibroblast) - GEIMM
IGF107/84 (skin, fibroblast, glycogen storage disease III) - GEIMM
IGF107/85 (skin, fibroblast) - GEIMM
IGF107/89 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF107/90 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF107/91 (skin, fibroblast) - GEIMM
IGF108/80 (skin, fibroblast) - GEIMM
IGF108/81 (skin, fibroblast, Gaucher disease type III) - GEIMM
IGF108/82 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF108/83 (skin, fibroblast, hyperammonemia due to carbamoylphosphate synthetase deficien.) - GEIMM
IGF108/84 (skin, fibroblast) - GEIMM
IGF108/85 (skin, fibroblast) - GEIMM
IGF108/90 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF108/91 (skin, fibroblast, methylmalonicacidemia) - GEIMM
IGF109/79 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF109/80 (skin, fibroblast) - GEIMM
IGF109/81 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF109/83 (skin, fibroblast) - GEIMM
IGF109/84 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF109/85 (skin, fibroblast, Laurence-Moon syndrome) - GEIMM
IGF109/91 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF110/78 (skin, fibroblast, homocystinuria) - GEIMM
IGF110/80 (skin, fibroblast) - GEIMM
IGF110/81 (skin, fibroblast) - GEIMM
IGF110/82 (skin, fibroblast, glycogen storage disease I) - GEIMM
IGF110/83 (skin, fibroblast) - GEIMM
IGF110/85 (skin, fibroblast, complex IV,mitocondrial respiratory chain,deficiency of) - GEIMM
IGF110/91 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF111/80 (skin, fibroblast, mucopolysaccharidosis type VI) - GEIMM
IGF111/82 (skin, fibroblast) - GEIMM
IGF111/83 (skin, fibroblast, galactose epimerase deficiency) - GEIMM
IGF111/84 (skin, fibroblast) - GEIMM
IGF111/85 (skin, fibroblast) - GEIMM
IGF111/90 (skin, fibroblast) - GEIMM
IGF112/80 (skin, fibroblast) - GEIMM
IGF112/81 (skin, fibroblast) - GEIMM
IGF112/82 (skin, fibroblast, maple syrup urine disease) - GEIMM
IGF112/83 (skin, fibroblast) - GEIMM
IGF112/84 (skin, fibroblast) - GEIMM
IGF112/85 (skin, fibroblast, gangliosidosis, generalized GM1, type II) - GEIMM
IGF112/87 (skin, fibroblast) - GEIMM
IGF112/91 (skin, fibroblast) - GEIMM
IGF113/80 (skin, fibroblast, Gaucher disease type II) - GEIMM
IGF113/81 (skin, fibroblast, methylmalonicacidemia) - GEIMM
IGF113/82 (skin, fibroblast) - GEIMM
IGF113/83 (skin, fibroblast, Berardinelli syndrome /seip syndrome) - GEIMM
IGF113/84 (skin, fibroblast) - GEIMM
IGF113/85 (skin, fibroblast, Marfan syndrome) - GEIMM
IGF113/87 (skin, fibroblast) - GEIMM
IGF113/91 (skin, fibroblast, mucopolysaccharidosis type III B) - GEIMM
IGF114/82 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF114/83 (skin, fibroblast) - GEIMM
IGF114/84 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF114/85 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF114/87 (skin, fibroblast) - GEIMM
IGF114/91 (skin, fibroblast) - GEIMM
IGF115/81 (skin, fibroblast) - GEIMM
IGF115/82 (skin, fibroblast) - GEIMM
IGF115/83 (skin, fibroblast) - GEIMM
IGF115/84 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF115/85 (skin, fibroblast) - GEIMM
IGF115/90 (skin, fibroblast, leprechaunism) - GEIMM
IGF115/91 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF116/81 (skin, fibroblast) - GEIMM
IGF116/82 (skin, fibroblast, Gaucher disease type II) - GEIMM
IGF116/83 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF116/84 (skin, fibroblast) - GEIMM
IGF116/85 (skin, fibroblast) - GEIMM
IGF116/91 (skin, fibroblast) - GEIMM
IGF117/80 (skin, fibroblast) - GEIMM
IGF117/81 (skin, fibroblast) - GEIMM
IGF117/83 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF117/84 (skin, fibroblast, fibrodysplasia ossificans progressiva) - GEIMM
IGF117/85 (skin, fibroblast, amaurotic family idiocy, late infantile type/NCL late infantile) - GEIMM
IGF117/91 (skin, fibroblast, osteogenesis imperfecta) - GEIMM
IGF118/80 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF118/81 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF118/82 (skin, fibroblast) - GEIMM
IGF118/84 (skin, fibroblast) - GEIMM
IGF118/85 (skin, fibroblast) - GEIMM
IGF118/91 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF119/83 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF119/84 (skin, fibroblast) - GEIMM
IGF119/85 (skin, fibroblast) - GEIMM
IGF119/91 (skin, fibroblast) - GEIMM
IGF120/81 (skin, fibroblast, maple syrup urine disease) - GEIMM
IGF120/82 (skin, fibroblast) - GEIMM
IGF120/83 (skin, fibroblast, triglyceride storage disease) - GEIMM
IGF120/84 (skin, fibroblast, fucosidosis) - GEIMM
IGF120/85 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF120/91 (skin, fibroblast) - GEIMM
IGF121/80 (skin, fibroblast) - GEIMM
IGF121/82 (skin, fibroblast) - GEIMM
IGF121/83 (skin, fibroblast) - GEIMM
IGF121/84 (skin, fibroblast) - GEIMM
IGF121/85 (skin, fibroblast) - GEIMM
IGF121/91 (skin, fibroblast, mucopolysaccharidosis type III C) - GEIMM
IGF122/82 (skin, fibroblast) - GEIMM
IGF122/83 (skin, fibroblast) - GEIMM
IGF122/84 (skin, fibroblast, Turner syndrome/noonan syndrome 1) - GEIMM
IGF122/85 (skin, fibroblast) - GEIMM
IGF122/91 (skin, fibroblast, pyruvate dehydrogenase def.) - GEIMM
IGF123/80 (skin, fibroblast) - GEIMM
IGF123/81 (skin, fibroblast) - GEIMM
IGF123/82 (skin, fibroblast) - GEIMM
IGF123/83 (skin, fibroblast) - GEIMM
IGF123/84 (skin, fibroblast) - GEIMM
IGF123/85 (skin, fibroblast) - GEIMM
IGF123/91 (skin, fibroblast, Krabbe disease) - GEIMM
IGF124/80 (skin, fibroblast) - GEIMM
IGF124/81 (skin, fibroblast, xeroderma pigmentosum I) - GEIMM
IGF124/82 (skin, fibroblast, Jarcho-Levin syndrome) - GEIMM
IGF124/84 (skin, fibroblast, Sandhoff disease) - GEIMM
IGF124/85 (skin, fibroblast) - GEIMM
IGF124/91 (skin, fibroblast) - GEIMM
IGF125/80 (skin, fibroblast) - GEIMM
IGF125/81 (skin, fibroblast, xeroderma pigmentosum I) - GEIMM
IGF125/82 (skin, fibroblast, dibasicaminoaciduria II) - GEIMM
IGF125/84 (skin, fibroblast, fibrodysplasia ossificans progressiva) - GEIMM
IGF125/85 (skin, fibroblast) - GEIMM
IGF126/80 (skin, fibroblast) - GEIMM
IGF126/81 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF126/83 (skin, fibroblast) - GEIMM
IGF126/84 (skin, fibroblast) - GEIMM
IGF126/85 (skin, fibroblast) - GEIMM
IGF126/91 (skin, fibroblast, congenital undergrowth of left leg) - GEIMM
IGF127/80 (skin, fibroblast) - GEIMM
IGF127/82 (skin, fibroblast, Alexander disease) - GEIMM
IGF127/83 (skin, fibroblast) - GEIMM
IGF127/85 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF127/91 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF128/80 (skin, fibroblast) - GEIMM
IGF128/83 (skin, fibroblast) - GEIMM
IGF128/84 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF128/85 (skin, fibroblast) - GEIMM
IGF128/91 (skin, fibroblast, adrenal gland tumor) - GEIMM
IGF129/80 (skin, fibroblast, mucopolysaccharidosis type VI) - GEIMM
IGF129/82 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF129/84 (skin, fibroblast) - GEIMM
IGF130/82 (skin, fibroblast, tyrosine transaminase deficiency) - GEIMM
IGF130/83 (skin, fibroblast, Lesch-Nyhan syndrome) - GEIMM
IGF130/84 (skin, fibroblast) - GEIMM
IGF130/91 (skin, fibroblast, B1 variant - GM2 gangliosidosis / Tay-Sachs disease) - GEIMM
IGF131/80 (skin, fibroblast, propionicacidemia I) - GEIMM
IGF131/82 (skin, fibroblast) - GEIMM
IGF131/83 (skin, fibroblast, dystonia musculorum deformans 2) - GEIMM
IGF131/84 (skin, fibroblast) - GEIMM
IGF132/80 (skin, fibroblast, Charcot-Marie-Tooth disease) - GEIMM
IGF132/82 (skin, fibroblast) - GEIMM
IGF132/83 (skin, fibroblast) - GEIMM
IGF133/80 (skin, fibroblast) - GEIMM
IGF133/82 (skin, fibroblast) - GEIMM
IGF133/83 (skin, fibroblast) - GEIMM
IGF134/82 (skin, fibroblast, fucosidosis) - GEIMM
IGF134/83 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF135/80 (skin, fibroblast) - GEIMM
IGF135/82 (skin, fibroblast, spongy degeneration of central nervous system /Canavan disease) - GEIMM
IGF135/83 (skin, fibroblast, angiokeratoma, diffuse / Fabry disease) - GEIMM
IGF136/80 (skin, fibroblast) - GEIMM
IGF136/82 (skin, fibroblast) - GEIMM
IGF136/83 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF137/80 (skin, fibroblast, Charcot-Marie-Tooth disease) - GEIMM
IGF137/83 (skin, fibroblast, angiokeratoma, diffuse / Fabry disease) - GEIMM
IGF138/80 (skin, fibroblast) - GEIMM
IGF138/82 (skin, fibroblast, Wolman disease/cholesterol ester storage disease) - GEIMM
IGF138/83 (skin, fibroblast) - GEIMM
IGF139/80 (skin, fibroblast, Charcot-Marie-Tooth disease) - GEIMM
IGF139/83 (skin, fibroblast) - GEIMM
IGF140/80 (skin, fibroblast) - GEIMM
IGF140/83 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF141/80 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF141/82 (skin, fibroblast, xerodermic idiocy of De Sanctis and Cacchione) - GEIMM
IGF141/83 (skin, fibroblast, trisomy 21 / Down syndrome) - GEIMM
IGF142/80 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF142/83 (skin, fibroblast) - GEIMM
IGF143/80 (skin, fibroblast) - GEIMM
IGF143/82 (skin, fibroblast, phenylketonuria I) - GEIMM
IGF143/83 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF144/80 (skin, fibroblast, cystic fibrosis) - GEIMM
IGF144/82 (skin, fibroblast, phenylketonuria I) - GEIMM
IGF144/83 (skin, fibroblast) - GEIMM
IGF145/80 (skin, fibroblast) - GEIMM
IGF145/83 (skin, fibroblast) - GEIMM
IGF146/80 (skin, fibroblast, ornithine-transcarbamylase deficiency) - GEIMM
IGF146/82 (skin, fibroblast, sialic acid storage disease) - GEIMM
IGF147/82 (skin, fibroblast) - GEIMM
IGF147/83 (skin, fibroblast) - GEIMM
IGF148/82 (skin, fibroblast) - GEIMM
IGF148/83 (skin, fibroblast) - GEIMM
IGF149/82 (skin, fibroblast) - GEIMM
IGF149/83 (skin, fibroblast, mucopolysaccharidosis type IV B / Morquio syndrome) - GEIMM
IGF150/83 (skin, fibroblast) - GEIMM
IGF151/82 (skin, fibroblast) - GEIMM
IGF151/83 (skin, fibroblast) - GEIMM
IGF152/82 (skin, fibroblast) - GEIMM
IGF152/83 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF153/82 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF153/83 (skin, fibroblast) - GEIMM
IGF154/82 (skin, fibroblast) - GEIMM
IGF154/83 (skin, fibroblast, glycogen storage disease III) - GEIMM
IGF155/82 (skin, fibroblast) - GEIMM
IGF156/82 (skin, fibroblast, xerodermic idiocy of De Sanctis and Cacchione) - GEIMM
IGF156/83 (skin, fibroblast) - GEIMM
IGF157/82 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF157/83 (skin, fibroblast) - GEIMM
IGF158/82 (skin, fibroblast, sponastrime dysplasia) - GEIMM
IGF158/83 (skin, fibroblast) - GEIMM
IGF159/82 (skin, fibroblast) - GEIMM
IGF159/83 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF160/82 (skin, fibroblast, Niemann-Pick disease, type B) - GEIMM
IGF160/83 (skin, fibroblast, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF161/83 (skin, fibroblast, propionicacidemia I) - GEIMM
IGF162/83 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF163/83 (skin, fibroblast, Gaucher disease type III) - GEIMM
IGF164/83 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF165/83 (skin, fibroblast) - GEIMM
IGF166/83 (skin, fibroblast, trichothiodystrophy) - GEIMM
IGF168/83 (skin, fibroblast) - GEIMM
IGF169/83 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF170/83 (skin, fibroblast) - GEIMM
IGF171/83 (skin, fibroblast) - GEIMM
IGF172/83 (skin, fibroblast) - GEIMM
IGF173/83 (skin, fibroblast) - GEIMM
IGF174/83 (skin, fibroblast) - GEIMM
IGF175/83 (skin, fibroblast) - GEIMM
IGF176/83 (skin, fibroblast) - GEIMM
IGF177/83 (skin, fibroblast) - GEIMM
IGF178/83 (skin, fibroblast) - GEIMM
IGF179/83 (skin, fibroblast) - GEIMM
IGF180/83 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF181/83 (skin, fibroblast, mannosidosis, alpha b, lysosomal) - GEIMM
IGF182/83 (skin, fibroblast, gangliosidosis, generalized GM1, type II) - GEIMM
IGF183/83 (skin, fibroblast, Turner syndrome/noonan syndrome 1) - GEIMM
IGF186/83 (skin, fibroblast) - GEIMM
IGF187/83 (skin, fibroblast, hyperglycinemia, nonketotic) - GEIMM
IGF200/83 (skin, fibroblast) - GEIMM
IGF201/83 (skin, fibroblast) - GEIMM
IGF740/88 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGL001/01 (lymphoblast) - GEIMM
IGL001/91 (lymphoblast, mucopolysaccharidosis type II) - GEIMM
IGL001/92 (lymphoblast, mucopolysaccharidosis type II) - GEIMM
IGL001/93 (lymphoblast, fucosidosis) - GEIMM
IGL001/95 (lymphoblast) - GEIMM
IGL001/96 (lymphoblast, Wolman disease/cholesterol ester storage disease) - GEIMM
IGL001/97 (lymphoblast) - GEIMM
IGL001/98 (lymphoblast) - GEIMM
IGL001/99 (lymphoblast) - GEIMM
IGL002/00 (lymphoblast) - GEIMM
IGL002/01 (lymphoblast) - GEIMM
IGL002/91 (lymphoblast) - GEIMM
IGL002/92 (lymphoblast, Aicardi syndrome / corpus callosum) - GEIMM
IGL002/93 (lymphoblast, fucosidosis) - GEIMM
IGL002/94 (lymphoblast) - GEIMM
IGL002/96 (lymphoblast) - GEIMM
IGL002/98 (lymphoblast) - GEIMM
IGL002/99 (lymphoblast) - GEIMM
IGL003/00 (lymphoblast) - GEIMM
IGL003/01 (lymphoblast) - GEIMM
IGL003/91 (lymphoblast) - GEIMM
IGL003/92 (lymphoblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGL003/93 (lymphoblast) - GEIMM
IGL003/95 (lymphoblast, glycogen storage disease II) - GEIMM
IGL003/96 (lymphoblast, Berardinelli syndrome /seip syndrome) - GEIMM
IGL003/97 (lymphoblast) - GEIMM
IGL003/98 (lymphoblast) - GEIMM
IGL003/99 (lymphoblast, methylenetetra-hydrofolate reductase def.) - GEIMM
IGL004/00 (lymphoblast) - GEIMM
IGL004/01 (lymphoblast) - GEIMM
IGL004/91 (lymphoblast) - GEIMM
IGL004/93 (lymphoblast) - GEIMM
IGL004/94 (lymphoblast, autoimmune polyendocrinopathy syndrome,type I) - GEIMM
IGL004/96 (lymphoblast) - GEIMM
IGL004/97 (lymphoblast) - GEIMM
IGL004/98 (lymphoblast) - GEIMM
IGL004/99 (lymphoblast, Gaucher disease type I) - GEIMM
IGL005/00 (lymphoblast) - GEIMM
IGL005/01 (lymphoblast) - GEIMM
IGL005/91 (lymphoblast, mucopolysaccharidosis type III B) - GEIMM
IGL005/92 (lymphoblast, articular hypermobility syndrome) - GEIMM
IGL005/93 (lymphoblast, mucopolysaccharidosis type II) - GEIMM
IGL005/95 (lymphoblast) - GEIMM
IGL005/97 (lymphoblast) - GEIMM
IGL005/98 (lymphoblast, Niemann-Pick disease, type A) - GEIMM
IGL005/99 (lymphoblast) - GEIMM
IGL006/00 (lymphoblast) - GEIMM
IGL006/01 (lymphoblast) - GEIMM
IGL006/92 (lymphoblast) - GEIMM
IGL006/93 (lymphoblast) - GEIMM
IGL006/95 (lymphoblast) - GEIMM
IGL006/97 (lymphoblast) - GEIMM
IGL006/98 (lymphoblast, glycogen storage disease II) - GEIMM
IGL006/99 (lymphoblast, Gaucher disease type I) - GEIMM
IGL007/00 (lymphoblast) - GEIMM
IGL007/01 (lymphoblast) - GEIMM
IGL007/91 (lymphoblast, Krabbe disease) - GEIMM
IGL007/92 (lymphoblast) - GEIMM
IGL007/94 (lymphoblast, Gaucher disease type I) - GEIMM
IGL007/96 (lymphoblast) - GEIMM
IGL007/98 (lymphoblast, Gaucher disease type I) - GEIMM
IGL007/99 (lymphoblast, Gaucher disease type I) - GEIMM
IGL008/00 (lymphoblast, salla disease) - GEIMM
IGL008/92 (lymphoblast, mucopolysaccharidosis type II) - GEIMM
IGL008/93 (lymphoblast, Alagille syndrome) - GEIMM
IGL008/94 (lymphoblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGL008/96 (lymphoblast) - GEIMM
IGL008/98 (lymphoblast) - GEIMM
IGL008/99 (lymphoblast, Gaucher disease type I) - GEIMM
IGL009/00 (lymphoblast) - GEIMM
IGL009/01 (lymphoblast) - GEIMM
IGL009/92 (lymphoblast, mucopolysaccharidosis type II) - GEIMM
IGL009/96 (lymphoblast, acyl-CoA dehydrogenase, long-chain, deficiency) - GEIMM
IGL009/97 (lymphoblast) - GEIMM
IGL009/99 (lymphoblast, Gaucher disease type I) - GEIMM
IGL010/00 (lymphoblast) - GEIMM
IGL010/92 (lymphoblast) - GEIMM
IGL010/94 (lymphoblast) - GEIMM
IGL010/98 (lymphoblast) - GEIMM
IGL010/99 (lymphoblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGL011/00 (lymphoblast) - GEIMM
IGL011/01 (lymphoblast) - GEIMM
IGL011/96 (lymphoblast) - GEIMM
IGL011/97 (lymphoblast) - GEIMM
IGL011/98 (lymphoblast, Gaucher disease type I) - GEIMM
IGL011/99 (lymphoblast, mucopolysaccharidosis type III A) - GEIMM
IGL012/00 (lymphoblast) - GEIMM
IGL012/01 (lymphoblast) - GEIMM
IGL012/95 (lymphoblast, Wolman disease/cholesterol ester storage disease) - GEIMM
IGL012/97 (lymphoblast) - GEIMM
IGL012/98 (lymphoblast) - GEIMM
IGL012/99 (lymphoblast) - GEIMM
IGL013/00 (lymphoblast) - GEIMM
IGL013/01 (lymphoblast) - GEIMM
IGL013/95 (lymphoblast) - GEIMM
IGL013/96 (lymphoblast) - GEIMM
IGL013/97 (lymphoblast) - GEIMM
IGL013/98 (lymphoblast, mucopolysaccharidosis type III C) - GEIMM
IGL013/99 (lymphoblast) - GEIMM
IGL014/00 (lymphoblast, Gaucher disease type I) - GEIMM
IGL014/01 (lymphoblast) - GEIMM
IGL014/95 (lymphoblast) - GEIMM
IGL014/96 (lymphoblast) - GEIMM
IGL014/97 (lymphoblast) - GEIMM
IGL014/98 (lymphoblast, Niemann-Pick disease, type A) - GEIMM
IGL014/99 (lymphoblast, mucopolysaccharidosis type II) - GEIMM
IGL015/00 (lymphoblast) - GEIMM
IGL015/01 (lymphoblast) - GEIMM
IGL015/96 (lymphoblast) - GEIMM
IGL015/97 (lymphoblast) - GEIMM
IGL015/98 (lymphoblast) - GEIMM
IGL015/99 (lymphoblast) - GEIMM
IGL016/00 (lymphoblast) - GEIMM
IGL016/01 (lymphoblast) - GEIMM
IGL016/96 (lymphoblast) - GEIMM
IGL016/97 (lymphoblast) - GEIMM
IGL016/98 (lymphoblast) - GEIMM
IGL016/99 (lymphoblast, Gaucher disease type I) - GEIMM
IGL017/00 (lymphoblast) - GEIMM
IGL017/01 (lymphoblast) - GEIMM
IGL017/96 (lymphoblast, glycogen storage disease II) - GEIMM
IGL017/97 (lymphoblast) - GEIMM
IGL017/98 (lymphoblast, mucopolysaccharidosis type IV A) - GEIMM
IGL017/99 (lymphoblast) - GEIMM
IGL018/96 (lymphoblast) - GEIMM
IGL018/97 (lymphoblast) - GEIMM
IGL018/98 (lymphoblast, Gaucher disease type II) - GEIMM
IGL018/99 (lymphoblast) - GEIMM
IGL019/00 (lymphoblast) - GEIMM
IGL019/96 (lymphoblast) - GEIMM
IGL019/97 (lymphoblast) - GEIMM
IGL019/98 (lymphoblast, Gaucher disease type II) - GEIMM
IGL019/99 (lymphoblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGL020/96 (lymphoblast) - GEIMM
IGL020/98 (lymphoblast, Wolman disease/cholesterol ester storage disease) - GEIMM
IGL020/99 (lymphoblast) - GEIMM
IGL021/96 (lymphoblast) - GEIMM
IGL021/98 (lymphoblast) - GEIMM
IGL021/99 (lymphoblast) - GEIMM
IGL022/00 (lymphoblast) - GEIMM
IGL022/96 (lymphoblast) - GEIMM
IGL022/98 (lymphoblast) - GEIMM
IGL022/99 (lymphoblast) - GEIMM
IGL023/00 (lymphoblast) - GEIMM
IGL023/96 (lymphoblast) - GEIMM
IGL023/98 (lymphoblast) - GEIMM
IGL023/99 (lymphoblast) - GEIMM
IGL024/00 (lymphoblast) - GEIMM
IGL024/96 (lymphoblast) - GEIMM
IGL024/98 (lymphoblast, Gaucher disease type I) - GEIMM
IGL024/99 (lymphoblast) - GEIMM
IGL025/00 (lymphoblast, SURF1) - GEIMM
IGL025/98 (lymphoblast, mucopolysaccharidosis type IV A) - GEIMM
IGL025/99 (lymphoblast) - GEIMM
IGL026/00 (lymphoblast) - GEIMM
IGL026/99 (lymphoblast) - GEIMM
IGL027/00 (lymphoblast) - GEIMM
IGL027/98 (lymphoblast, neuropathy, giant axonal) - GEIMM
IGL027/99 (lymphoblast) - GEIMM
IGL028/00 (lymphoblast) - GEIMM
IGL028/98 (lymphoblast, Gaucher disease type III) - GEIMM
IGL028/99 (lymphoblast) - GEIMM
IGL029/00 (lymphoblast, Gaucher disease type I) - GEIMM
IGL029/98 (lymphoblast) - GEIMM
IGL029/99 (lymphoblast) - GEIMM
IGL030/00 (lymphoblast, Gaucher disease type II) - GEIMM
IGL030/98 (lymphoblast) - GEIMM
IGL030/99 (lymphoblast) - GEIMM
IGL031/00 (lymphoblast) - GEIMM
IGL031/98 (lymphoblast) - GEIMM
IGL031/99 (lymphoblast, Gaucher disease type I) - GEIMM
IGL032/00 (lymphoblast) - GEIMM
IGL032/98 (lymphoblast) - GEIMM
IGL032/99 (lymphoblast) - GEIMM
IGL033/00 (lymphoblast) - GEIMM
IGL033/98 (lymphoblast) - GEIMM
IGL033/99 (lymphoblast) - GEIMM
IGL034/00 (lymphoblast, Niemann-Pick disease, type C) - GEIMM
IGL034/99 (lymphoblast) - GEIMM
IGL035/00 (lymphoblast, spastic paraparesis) - GEIMM
IGL035/99 (lymphoblast) - GEIMM
IGL036/99 (lymphoblast) - GEIMM
IGL037/99 (lymphoblast) - GEIMM
IGL038/99 (lymphoblast) - GEIMM
IGL039/99 (lymphoblast) - GEIMM
IGL040/99 (lymphoblast) - GEIMM
IGL041/99 (lymphoblast) - GEIMM
IGV001/92 (chorionic villi, glycogen storage disease II) - GEIMM
IGV001/96 (chorionic villi, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGV001/99 (chorionic villi, mucolipidosis II) - GEIMM
IGV003/90 (chorionic villi, Tay-Sachs disease) - GEIMM
IGV003/93 (chorionic villi, fucosidosis) - GEIMM
IGV005/93 (chorionic villi, Niemann-Pick disease, type A) - GEIMM
IGV005/94 (chorionic villi, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGV006/99 (chorionic villi, Gaucher disease type II) - GEIMM
IGV008/94 (chorionic villi, mucolipidosis II) - GEIMM
IGV009/90 (chorionic villi, metachromatic leukodystrophy, late-infantile) - GEIMM
IGV009/96 (chorionic villi, Gaucher disease type II) - GEIMM
IGV009/99 (chorionic villi, Krabbe disease) - GEIMM
IGV011/92 (chorionic villi, Sjogren-Larsson syndrome) - GEIMM
IGV017/91 (chorionic villi, mucopolysaccharidosis type II) - GEIMM
IGV025/91 (chorionic villi, mucopolysaccharidosis type II) - GEIMM
IGV028/91 (chorionic villi, gangliosidosis, generalized GM1, type I) - GEIMM
IGV029/91 (chorionic villi, glycogen storage disease II) - GEIMM
IGV030/84 (chorionic villi, gangliosidosis, generalized GM1, type I) - GEIMM
IGV032/91 (chorionic villi, Sandhoff disease) - GEIMM
IM 9 (bone marrow, multiple myeloma) - ECACC
IM-9 (bone marrow, multiple myeloma) - IZSBS
IM-9 (bone marrow, multiple myeloma) - SPBIC
IMR 32 (abdomen, neuroblastoma) - ECACC
IMR 32 (neuroblastoma) - IZSBS
IMR-32 (neuroblastoma) - BOHIC
IMR-32 (neuroblastoma) - DSMZ
IMR-32 (neuroblastoma) - GEICV
IMR-32 (neuroblastoma) - ICLC
IMR-32 (neuroblastoma) - MIISA
IMR-32 (neuroblastoma) - MIUEP
IMR-32 (neuroblastoma) - RMUPG
IMR-32 (neuroblastoma) - SPBIC
IMR-5 (neuroblastoma) - ICLC
IMR-90 (lung, embryonic) - ECACC
IMR-90 (lung, embryonic) - IZSBS
INT 407 (intestine, embryonic) - ECACC
Intestine 407 (intestine, embryonic) - IZSBS
Intestine 407 (intestine, embryonic) - MIUCC
Intestine 407 (intestine, embryonic) - PRUMB
IP1PV (skin, fibroblast, incontinentia pigmenti) - PVCGU
IP2PV (skin, fibroblast) - PVCGU
IS94 (lymphocyte) - GGB
IST-EBV-TW6A (lymphocyte, B) - ICLC
IST-EBV-TW6B (lymphocyte, B) - ICLC
IST-MEL1 (skin, melanoma) - ICLC
IST-MEL2 (skin, melanoma) - ICLC
IST-MEL3 (skin, melanoma) - ICLC
IST-MES1 (pleural effusion, mesothelioma) - ICLC
IST-MES2 (pleural effusion, mesothelioma) - ICLC
IV95 (lymphocyte, trisomy 21 / Down syndrome) - GGB
J-96 (peripheral blood, leukemia, subacute) - MWIIW
Ja Bos (skin, fibroblast, Ehlers-Danlos syndrome) - BGEBS
Jay Sen (skin, fibroblast, Ehlers-Danlos syndrome, type I) - BGEBS
JVM-13 (blood, leukemia, B-prolymphocytic) - ECACC
K 562 (pleural effusion, leukemia, chronic myeloid) - IZSBS
K-562 (pleural effusion, leukemia, chronic myeloid) - ANIIR
K-562 (pleural effusion, leukemia, chronic myeloid) - BOHIC
K-562 (pleural effusion, leukemia, chronic myeloid) - CHUIM
K-562 (pleural effusion, leukemia, myelogenous) - ICLC
K-562 (pleural effusion, leukemia, chronic myeloid) - MIEOS
K-562 (pleural effusion, leukemia, chronic myeloid) - MIISB
K-562 (pleural effusion, leukemia, chronic myeloid) - MWIIW
K-562 (pleural effusion, leukemia, chronic myeloid) - PNIOS
K-562 (pleural effusion, leukemia, chronic myeloid) - RMEBA
K-562 (pleural effusion, leukemia, chronic myeloid) - RMUFM
K-562 (pleural effusion, leukemia, chronic myeloid) - SPBIC
K562 (blood, leukemia, chronic myeloid) - ECACC
K562 cl.6 (blood, leukemia, chronic myeloid) - ECACC
KB (cervix, carcinoma) - DSMZ
KB (mouth, carcinoma, epidermoid) - ECACC
KB (mouth, carcinoma, squamous cell) - IZSBS
KB (mouth, carcinoma, squamous cell) - MWIIW
KB (mouth, carcinoma, squamous cell) - PRUMB
KB (mouth, carcinoma, squamous cell) - SPBIC
KG-1 (bone marrow, leukemia, acute myeloid) - BOHIC
KG-1 (bone marrow, leukemia, acute myeloid) - ECACC
KG-1 (bone marrow, leukemia, acute myeloid) - SPBIC
KG-1a (bone marrow, leukemia, acute myeloid) - PNIOS
KG1a (bone marrow, leukemia, acute myeloid) - ECACC
KHOS-240S (bone, osteosarcoma) - ECACC
KHOS-312H (bone, osteosarcoma) - ECACC
KHOS/NP (bone, osteosarcoma) - ECACC
KHOS/NP (bone, osteosarcoma) - IZSBS
L-A86 (amnion, trisomy 21 / Down syndrome) - GGB
L-C90 (amnion, hydrocephalus) - GGB
L-DR92a (amnion, chromosome aberration) - GGB
L-DR92f (fibroblast, chromosome aberration) - GGB
L-F95 (amnion) - GGB
L-M92 (amnion, trisomy 21 / Down syndrome) - GGB
L-V91 (amnion, Miller-Dieker syndrome) - GGB
L-V94 (amnion, trisomy 21 / Down syndrome) - GGB
L-Z93a (amnion, chromosome aberration) - GGB
L-Z93f (fibroblast) - GGB
L1192 (fibroblast, Patau syndrome / trisomy 13) - GGB
L1296 (fibroblast, trisomy 21 / Down syndrome) - GGB
L89M (lymphocyte) - GGB
L89P (lymphocyte) - GGB
L90 (lymphocyte, Huntington chorea) - GGB
L94 (fibroblast, Dyskeratosis congenita) - GGB
LA92 (skin, epidermolysis bullo'sa) - GGB
LA96 (lymphocyte, tuberous sclerosis) - GGB
LAN-188 (neuroblastoma) - GGB
LAn96 (lymphocyte, tuberous sclerosis) - GGB
Lb 224 (lymphocyte) - NAUBC
Lb 23 (lymphocyte, mucopolysaccharidosis type II) - NAUBC
Lb 24 (lymphocyte, mucopolysaccharidosis type II) - NAUBC
Lb 752 (lymphocyte, mucopolysaccharidosis type III B) - NAUBC
LBE88 (lymphocyte) - GGB
LL29 (AnHa) (lung, pulmonary fibrosis, idiopathic) - ECACC
LL86 (LeSa) (lung, sarcoma, osteogenic) - ECACC
LM 1 (skin, fibroblast) - BGEBS
LM 10 (skin, fibroblast) - BGEBS
LM 11 (skin, fibroblast, epidermolysis bullo'sa dystrophica, recessive) - BGEBS
LM 12 (skin, fibroblast) - BGEBS
LM 13 (skin, fibroblast) - BGEBS
LM 2 (skin, fibroblast, Ehlers-Danlos syndrome) - BGEBS
LM 3 (skin, fibroblast, Ehlers-Danlos syndrome) - BGEBS
LM 4 (skin, fibroblast) - BGEBS
LM 5 (skin, fibroblast) - BGEBS
LM 6 (skin, fibroblast) - BGEBS
LM 7 (skin, fibroblast) - BGEBS
LM 8 (skin, fibroblast, Ehlers-Danlos syndrome) - BGEBS
LM 9 (skin, fibroblast, Ehlers-Danlos syndrome) - BGEBS
LM-M92 (amnion, trisomy 21 / Down syndrome) - GGB
LM96 (lymphocyte, tuberous sclerosis) - GGB
LMas96 (lymphocyte, tuberous sclerosis) - GGB
LNCap.FGC (prostate, adenocarcinoma) - ICLC
LNCaP.FGC (prostate, carcinoma) - IZSBS
LNCaP.FGC (prostate, adenocarcinoma) - MIUEP
LoVo (colon, adenocarcinoma) - ECACC
LoVo (colon, adenocarcinoma) - ICLC
LoVo (colon, adenocarcinoma) - MIEOS
LoVo (colon, adenocarcinoma) - MIISB
LP96 (lymphocyte, tuberous sclerosis) - GGB
LS 123 (colon, adenocarcinoma) - ECACC
LS 180 (colon, adenocarcinoma) - IZSBS
LS-180 (colon, adenocarcinoma, colorectal) - ICLC
LS180 (colon, adenocarcinoma) - ECACC
LT89 (lymphocyte, Martin-Bell syndrome) - GGB
LT94 (lymphocyte, Fanconi anemia) - GGB
LUDLU-1 (lung, carcinoma, squamous cell) - ECACC
M-07e (peripheral blood, leukemia, acute megakaryoblastic) - ICLC
M-B87a (amnion, Edwards' syndrome / trisomy 18) - GGB
M-B87f (fibroblast, Edwards' syndrome / trisomy 18) - GGB
M-B95a (amnion, trisomy 21 / Down syndrome) - GGB
M-B95f (fibroblast, trisomy 21 / Down syndrome) - GGB
M-C95 (amnion, trisomy 21 / Down syndrome) - GGB
M-F92 (amnion, Patau syndrome / trisomy 13) - GGB
M-G89 (lymphocyte, chromosome aberration) - GGB
M-G93 (amnion, trisomy 21 / Down syndrome) - GGB
M-L94 (fibroblast) - GGB
M-L95a (amnion, trisomy 21 / Down syndrome) - GGB
M-L95f (fibroblast, trisomy 21 / Down syndrome) - GGB
M-M196 (fibroblast, trisomy 21 / Down syndrome) - GGB
M-M96 (amnion, trisomy 21 / Down syndrome) - GGB
M-N91 (amnion, trisomy 21 / Down syndrome) - GGB
M-P88 (amnion, trisomy 21 / Down syndrome) - GGB
M-P91a (amnion, Fanconi anemia) - GGB
M-P91f (fibroblast, Fanconi anemia) - GGB
M-R89 (fibroblast, trisomy 21 / Down syndrome) - GGB
M-R95 (amnion) - GGB
M-T95a (amnion) - GGB
M-T95f (fibroblast) - GGB
M-V94 (fibroblast, trisomy 21 / Down syndrome) - GGB
M0092 (trophoblast, chromosome aberration) - GGB
M1191 (chorionic villi, trisomy 9) - GGB
M1392 (fibroblast, chromosome aberration) - GGB
M1594 (fibroblast) - GGB
M83 (fibroblast) - GGB
M85 (fibroblast, hermaphroditism true) - GGB
M86 (fibroblast, anencephaly) - GGB
M90 (fibroblast) - GGB
MA86 (lymphocyte, trisomy 21 / Down syndrome) - GGB
MA91 (fibroblast, Fanconi anemia) - GGB
MA94IL2 (lymphocyte, Fanconi anemia) - GGB
MA94LEBV (lymphocyte, Fanconi anemia) - GGB
MALME-3M (lung, metastasis, melanoma) - MIEOS
MAM94M (lymphocyte) - GGB
MC86 (lymphocyte, trisomy 21 / Down syndrome) - GGB
MC88 (fibroblast) - GGB
MC94 (lymphocyte) - GGB
MC96 (lymphocyte, trisomy 21 / Down syndrome) - GGB
MCF 7 (breast, adenocarcinoma) - IZSBS
MCF-7 (breast, adenocarcinoma) - DSMZ
MCF7 (breast, adenocarcinoma) - ECACC
MCF7 (breast, adenocarcinoma) - GEIAP
MCF7 (breast, adenocarcinoma) - ICLC
MCF7 (breast, adenocarcinoma) - MIEOS
MCF7 (breast, adenocarcinoma) - MIISB
MCF7 (breast, adenocarcinoma) - SPBIC
MCF7 (breast, adenocarcinoma) - TOUCI
MCF7-382 (breast, adenocarcinoma) - GEIBM
MCF7-382 (breast, adenocarcinoma) - ICLC
MCF7-422 (breast, adenocarcinoma) - GEIBM
MCF7-422 (breast, adenocarcinoma) - ICLC
MCF7-432 (breast, adenocarcinoma) - GEIBM
MCF7-432 (breast, adenocarcinoma) - ICLC
MCF7-488X1 (breast, adenocarcinoma) - GEIBM
MCF7-488X1 (breast, adenocarcinoma) - ICLC
MCF7-490X1 (breast, adenocarcinoma) - GEIBM
MCF7-490X1 (breast, adenocarcinoma) - ICLC
MCF7-492X1 (breast, adenocarcinoma) - ICLC
MCR96M (lymphocyte) - GGB
MCS94MIL2 (lymphocyte) - GGB
MCS94MLEBV (lymphocyte) - GGB
MCT95M (lymphocyte) - GGB
MD94PLEBV (lymphocyte) - GGB
MD94SIL2 (lymphocyte) - GGB
MD94SLEBV (lymphocyte) - GGB
MD95 (lymphocyte, Martin-Bell syndrome) - GGB
MDA-MB-134-VI (breast, carcinoma, ductal) - MIEOS
MDA-MB-231 (breast, adenocarcinoma) - ECACC
MDA-MB-231 (breast, adenocarcinoma) - GEIAP
MDA-MB-231 (breast, adenocarcinoma) - ICLC
MDA-MB-231 (breast, adenocarcinoma) - TOUCI
MDA-MB-361 (breast, adenocarcinoma) - ECACC
MDA-MB-415 (breast, adenocarcinoma) - MIEOS
MDA-MB-453 (breast, carcinoma) - ICLC
ME-180 (cervix, carcinoma, epidermoid) - ICLC
ME96 (lymphocyte) - GGB
ME96P (lymphocyte) - GGB
MES-SA (uterus, sarcoma) - ECACC
MES-SA (uterus, sarcoma) - ICLC
MES-SA/Dx-5 (uterus, sarcoma) - ECACC
MF92 (fibroblast, osteogenesis imperfecta) - GGB
MFE-280 (endometrium, adenocarcinoma, endometrial) - ECACC
MFE-296 (endometrium, adenocarcinoma, endometrial) - ECACC
MG96No (lymphocyte) - GGB
MGF89P (lymphocyte) - GGB
MGL95 (lymphocyte, Wolff mental retardation syndrome) - GGB
MGP96Na (lymphocyte) - GGB
MIA PaCa-2 (pancreas, carcinoma) - IZSBS
MIA PaCa-2 (pancreas, carcinoma) - SPBIC
MIA-Pa-Ca-2 (pancreas, carcinoma) - ECACC
ML86 (fibroblast) - GGB
ML87P (lymphocyte) - GGB
ML89S (lymphocyte) - GGB
MLA87M (lymphocyte) - GGB
MM87f (fibroblast) - GGB
MM87IL2 (lymphocyte) - GGB
MM87ls (lymphocyte) - GGB
MM96 (lymphocyte, Martin-Bell syndrome) - GGB
MN95 (lymphocyte, Martin-Bell syndrome) - GGB
MN96 (lymphocyte) - GGB
MNNG/HOS (TE85, Clone F-5) (bone, sarcoma, osteogenic) - ECACC
Mo-B (peripheral blood, leukemia, hairy cell) - ECACC
MOM89M (lymphocyte) - GGB
MP 1 (lymphocyte) - ECBR
MP 10 (lymphocyte) - ECBR
MP 12 (lymphocyte) - ECBR
MP 14 (lymphocyte) - ECBR
MP 3 (lymphocyte) - ECBR
MP 4 (lymphocyte) - ECBR
MP 5 (lymphocyte) - ECBR
MP 6 (lymphocyte) - ECBR
MP 8 (lymphocyte) - ECBR
MP 9 (lymphocyte) - ECBR
MP90 (lymphocyte) - GGB
MP95P (lymphocyte) - GGB
MPL96M (lymphocyte) - GGB
MR (skin, fibroblast) - MIUFC
MR87 (lymphocyte) - GGB
MS95 (lymphocyte) - GGB
MSTO-211H (mesothelioma) - ICLC
MT89 (lymphocyte) - GGB
N-A90 (amnion, trisomy 21 / Down syndrome) - GGB
N-B88 (amnion) - GGB
N-C96 (amnion, Patau syndrome / trisomy 13) - GGB
N92 (fibroblast, dwarfism thanatophoric) - GGB
NA95P (lymphocyte) - GGB
NC-37 (blood) - ECACC
NC-37 (peripheral blood, lymphoblast) - SPBIC
NC-NC (lymphoblastoid B cell) - DSMZ
NC95 (lymphocyte, trisomy 21 / Down syndrome) - GGB
NCI-H1650 (lung, adenocarcinoma, bronchioalveolar carcinoma) - ICLC
NCI-H322 (lung, carcinoma, bronchioalveolar) - ECACC
NCI-H358 (lung, carcinoma, bronchioalveolar) - ECACC
NCI-H716 (colon, adenocarcinoma) - TOUCI
NCI-H727 (lung, carcinoma, non small cell) - ECACC
NCI-H727 (lung, carcinoma, non small cell) - ICLC
NCI-H929 (multiple myeloma) - DSMZ
NCI-H929 (myeloma) - ECACC
NF96 (lymphocyte, hypercholesterolemia, familial) - GGB
NF96IL2 (lymphocyte, hypercholesterolemia, familial) - GGB
NG96 (lymphocyte, hypercholesterolemia, familial) - GGB
NG96IL2 (lymphocyte, hypercholesterolemia, familial) - GGB
NGM96 (neuroblastoma) - GGB
NGP96 (neuroblastoma) - GGB
NIH:OVCAR-3 (adenocarcinoma, ovary) - IZSBS
NIH:OVCAR-3 (ovary, adenocarcinoma) - MIEOS
NM94 (lymphocyte, chromosome aberration) - GGB
NM95 (lymphocyte) - GGB
NT2-D1 (testis, carcinoma, embryonal pluripotent) - ICLC
NTERA-2 clone D1 (lung, metastasis, carcinoma, embryonal pluripotent) - ECACC
NV96 (lymphocyte, hypercholesterolemia, familial) - GGB
NV96IL2 (lymphocyte, hypercholesterolemia, familial) - GGB
O-B94a (amnion, Edwards' syndrome / trisomy 18) - GGB
O-C94 (amnion, tetraphocomelia) - GGB
O1192 (chorionic villi, trisomy 4) - GGB
O88M (lymphocyte) - GGB
O88P (lymphocyte) - GGB
OE19 (oesophagus, carcinoma) - ECACC
OE21 (oesophagus, carcinoma, squamous cell) - ECACC
OE33 (oesophagus, carcinoma) - ECACC
OE47 (oesophagus, carcinoma, squamous cell) - ECACC
OE50 (oesophagus, adenocarcinoma) - ECACC
OL95 (lymphocyte, Steinert disease) - GGB
OM87 (lymphocyte, dimorphism) - GGB
OM87P (lymphocyte) - GGB
Or De (skin, fibroblast, Ehlers-Danlos syndrome, type III) - BGEBS
OT87M (lymphocyte) - GGB
OVCAR-3 (ovary, adenocarcinoma) - ICLC
OVCAR-3 (ovary, carcinoma) - MIISB
P-190 (amnion, Edwards' syndrome / trisomy 18) - GGB
P-B88 (amnion, trisomy 21 / Down syndrome) - GGB
P-B91 (amnion, chromosome aberration) - GGB
P-B92 (amnion, chromosome aberration) - GGB
P-C96 (amnion, Edwards' syndrome / trisomy 18) - GGB
P-D89 (amnion) - GGB
P-D91 (amnion) - GGB
P-D94a (amnion, trisomy 21 / Down syndrome) - GGB
P-G96 (amnion, Edwards' syndrome / trisomy 18) - GGB
P-L92 (amnion, chromosome aberration) - GGB
P-NC94 (amnion) - GGB
P-R90 (amnion) - GGB
P-S90 (fibroblast, trisomy 21 / Down syndrome) - GGB
P-S96 (amnion) - GGB
P0894 (fibroblast, Edwards' syndrome / trisomy 18) - GGB
P1095 (chorionic villi, trisomy 21 / Down syndrome) - GGB
P1192 (fibroblast, Turner syndrome/noonan syndrome 1) - GGB
P1286 (fibroblast, trisomy 21 / Down syndrome) - GGB
P1294 (fibroblast) - GGB
P1392 (chorionic villi, chromosome aberration) - GGB
P1393 (chorionic villi, chromosome aberration) - GGB
P1985a (amnion, chondrodysplasia) - GGB
P1985f (amnion, chondrodysplasia) - GGB
P2092 (fibroblast) - GGB
P2189 (fibroblast) - GGB
P2190 (fibroblast) - GGB
P2594 (chorionic villi) - GGB
P92 (amnion, Prune Belly syndrome) - GGB
P93 (amnion, Turner syndrome/noonan syndrome 1) - GGB
P95 (amnion, Apert syndrome) - GGB
PA-1 (ovary, teratocarcinoma) - ECACC
PA-1 (ovary, teratocarcinoma) - GEICH
PA-1 (ovary, teratocarcinoma) - ICLC
PA-1 (ovary, teratocarcinoma) - SPBIC
PA90P (lymphocyte) - GGB
PA94 (lymphocyte) - GGB
PA95P (lymphocyte) - GGB
PA96 (lymphocyte, hypercholesterolemia, familial) - GGB
PANC-1 (pancreas, carcinoma) - ECACC
PANC-1 (pancreas, carcinoma) - IZSBS
PANC-1 (pancreas, carcinoma) - SPBIC
PBR86M (lymphocyte) - GGB
PC-3 (prostate, adenocarcinoma, grade IV) - ECACC
PC-3 (prostate, adenocarcinoma, grade IV) - ICLC
PC1296 (fibroblast) - GGB
PCA90M (lymphocyte) - GGB
PCV87M (lymphocyte) - GGB
PE86P (lymphocyte) - GGB
PE96 (lymphocyte, exostoses) - GGB
PF187 (fibroblast, trisomy 21 / Down syndrome) - GGB
PF90F (lymphocyte) - GGB
PG91 (fibroblast, trisomy 21 / Down syndrome) - GGB
PGA86M (lymphocyte) - GGB
PI86 (lymphocyte, trisomy 21 / Down syndrome) - GGB
PL90 (lymphocyte) - GGB
PM195 (lymphocyte) - GGB
PM85 (fibroblast) - GGB
PM87f (fibroblast) - GGB
PM87IL2 (lymphocyte) - GGB
PM89 (lymphocyte, trisomy 21 / Down syndrome) - GGB
PM91 (fibroblast, Turner syndrome, mosaic) - GGB
PM95 (lymphocyte) - GGB
PMA95M (lymphocyte) - GGB
PN86 (lymphocyte, chromosome aberration) - GGB
PR82 (fibroblast) - GGB
PR86S (lymphocyte) - GGB
PS192 (amnion, Prune Belly syndrome) - GGB
PS87P (lymphocyte) - GGB
PS92 (fibroblast, Fanconi anemia) - GGB
PS94 (lymphocyte) - GGB
PS95 (lymphocyte, Melnick-Needles syndrome) - GGB
PV95 (lymphocyte) - GGB
PX92 (pseudoxanthoma elasticum) - GGB
Q-P96 (fibroblast, trisomy 21 / Down syndrome) - GGB
Q1785 (fibroblast) - GGB
QV-R94 (amnion, anencephaly) - GGB
R D (muscle, rhabdomyosarcoma, embryonal) - IZSBS
R-A95 (fibroblast, trisomy 21 / Down syndrome) - GGB
R-B92 (amnion, Edwards' syndrome / trisomy 18) - GGB
R-C95 (fibroblast, Patau syndrome / trisomy 13) - GGB
R-C95a (amnion, Patau syndrome / trisomy 13) - GGB
R-C96 (amnion) - GGB
R-DC90a (amnion, trisomy 21 / Down syndrome) - GGB
R-DC90f (fibroblast, trisomy 21 / Down syndrome) - GGB
R-G196 (amnion) - GGB
R-G94a (amnion, trisomy 21 / Down syndrome) - GGB
R-G94f (fibroblast, trisomy 21 / Down syndrome) - GGB
R-G96 (lymphocyte) - GGB
R-M94 (amnion) - GGB
R-M95 (amnion) - GGB
R-P 91a (amnion, trisomy 21 / Down syndrome) - GGB
R-P 91f (fibroblast, trisomy 21 / Down syndrome) - GGB
R-R92 (amnion) - GGB
R-S95 (fibroblast, trisomy 21 / Down syndrome) - GGB
R-T96 (amnion) - GGB
R1391 (fibroblast) - GGB
R1487 (fibroblast, anencephaly) - GGB
R86 (fibroblast, Fanconi anemia) - GGB
R95 (amnion) - GGB
RAMOS (RA.1) (lymphoma, Burkitt) - ECACC
RD (muscle, rhabdomyosarcoma, embryonal) - BGEBS
RD (muscle, rhabdomyosarcoma, embryonal) - BOHIC
RD (muscle, rhabdomyosarcoma, embryonal) - BOUCN
RD (muscle, rhabdomyosarcoma, embryonal) - ECACC
RD (muscle, rhabdomyosarcoma, embryonal) - MWIIW
RD (muscle, rhabdomyosarcoma, embryonal) - PGUPG
RD (muscle, rhabdomyosarcoma, embryonal) - RMUPG
RD (muscle, rhabdomyosarcoma, embryonal) - SPBIC
RD-ES (sarcoma, Ewing's) - DSMZ
RD-ES (humerus, sarcoma, Ewing's) - MIEOS
RD91 (fibroblast, Down syndrome, mosaic) - GGB
RFE88 (lymphocyte) - GGB
Ri-1 (blood, lymphoma, B cell) - ECACC
RM86 (lymphocyte, trisomy 21 / Down syndrome) - GGB
RM91 (fibroblast, Pallister Killian syndrome) - GGB
RMR96 (lymphocyte) - GGB
ROV-S (bone marrow) - ICLC
RP88 (fibroblast, collagen disease) - GGB
RPMI 1788 (peripheral blood) - ECACC
RPMI 1788 (peripheral blood) - IZSBS
RPMI 1788 (peripheral blood) - SPBIC
RPMI 6666 (peripheral blood, lymphoma, Hodgkin) - ECACC
RPMI 7666 (lymphoblast) - ECACC
RPMI-7951 (malignant melanoma) - DSMZ
RT4 (bladder, papilloma, transitional cell) - ECACC
RT4 (bladder, papilloma, transitional cell) - MWIIW
S-C88 (amnion, omphalocele) - GGB
S-C93 (amnion) - GGB
S-D92a (amnion, Turner syndrome/noonan syndrome 1) - GGB
S-D92f (fibroblast, Turner syndrome/noonan syndrome 1) - GGB
S-D92v (chorionic villi) - GGB
S-F95 (fibroblast, trisomy 21 / Down syndrome) - GGB
S-G87 (amnion) - GGB
S-G94 (fibroblast, trisomy 21 / Down syndrome) - GGB
S-L90a (amnion, trisomy 21 / Down syndrome) - GGB
S-L90f (fibroblast, trisomy 21 / Down syndrome) - GGB
S-L95a (amnion, trisomy 21 / Down syndrome) - GGB
S-L95f (fibroblast, trisomy 21 / Down syndrome) - GGB
S-N87 (amnion) - GGB
S-P95 (fibroblast, trisomy 21 / Down syndrome) - GGB
S-R96 (amnion) - GGB
S-T92a (amnion, Edwards' syndrome / trisomy 18) - GGB
S-T92f (amnion, Edwards' syndrome / trisomy 18) - GGB
S0095 (fibroblast) - GGB
S1088 (chorionic villi) - GGB
S1295 (chorionic villi, trisomy 16) - GGB
S1391 (fibroblast) - GGB
S1887 (fibroblast) - GGB
S2793 (fibroblast, multiple malformations) - GGB
SA87f (fibroblast, Down syndrome, mosaic) - GGB
SA87ls (lymphocyte, Down syndrome, mosaic) - GGB
SA88 (fibroblast) - GGB
SA88f (fibroblast, Fanconi anemia) - GGB
SA88ls (lymphocyte, Fanconi anemia) - GGB
SAOS-2 (bone, sarcoma, osteogenic) - DSMZ
Saos-2 (bone, osteosarcoma) - ICLC
Saos-2 (bone, osteosarcoma) - IZSBS
SaOS-2 (bone, osteosarcoma) - MIISB
SBC-2 (cervix, carcinoma) - DSMZ
SBC-7 (cervix, carcinoma) - DSMZ
SBV86M (lymphocyte) - GGB
SE95IL2 (lymphocyte) - GGB
SE95ls (lymphocyte) - GGB
SG88P (lymphocyte) - GGB
SG94 (lymphocyte) - GGB
SGA96M (fibroblast) - GGB
SH-SY5Y (bone marrow, neuroblastoma) - ECACC
SH-SY5Y (neuroblastoma) - ICLC
SH-SY5Y (bone marrow, neuroblastoma) - RMEBA
SIMA (neuroblastoma) - DSMZ
SK LU 1 (lung, adenocarcinoma, grade III) - ECACC
SK-BR-3 (breast, adenocarcinoma) - TOUCI
SK-HEP-1 (liver, adenocarcinoma) - BSUPG
SK-HEP-1 (liver, adenocarcinoma) - DSMZ
SK-HEP-1 (liver, adenocarcinoma) - ECACC
SK-HEP-1 (liver, adenocarcinoma) - SPBIC
SK-LU-1 (lung, adenocarcinoma, grade III, poorly differentiated) - ICLC
SK-LU-1 (lung, adenocarcinoma, grade III) - IZSBS
SK-MEL-24 (skin, melanoma) - ICLC
SK-MEL-30 (melanoma) - DSMZ
SK-MEL-5 (skin, melanoma) - ICLC
SK-N-BE(2) (bone marrow, neuroblastoma) - ECACC
SK-N-BE(2) (bone marrow, neuroblastoma) - ICLC
SK-N-MC (neuroblastoma) - BOHIC
SK-N-MC (neuroblastoma) - DSMZ
SK-N-MC (neuroblastoma) - MIISA
SK-N-MC (neuroblastoma) - MIUEP
SK-N-MC (neuroblastoma) - RMUPG
SK-N-MC (neuroblastoma) - SPBIC
SK-N-SH (bone marrow, neuroblastoma) - BOHIC
SK-N-SH (bone marrow, neuroblastoma) - ECACC
SK-N-SH (neuroblastoma) - ICLC
SK-N-SH (bone marrow, neuroblastoma) - MIISA
SK-N-SH (bone marrow, neuroblastoma) - MIUEP
SK-N-SH (bone marrow, neuroblastoma) - RMUPG
SK-NEP-1 (kidney, Wilms' tumor) - IZSBS
SK-OV-3 (ovary, adenocarcinoma) - ECACC
SK-OV-3 (ovary, adenocarcinoma) - ICLC
SK-OV-3 (ovary, adenocarcinoma) - IZSBS
SK-OV-3 (ovary, adenocarcinoma) - MIISB
SK-UT-1B (mixed, leiomyosarcoma grade III) - SPBIC
SLC87M (lymphocyte) - GGB
SM86P (lymphocyte) - GGB
SM96P (fibroblast) - GGB
SMC87 (lymphocyte) - GGB
SMC95S (lymphocyte) - GGB
SP87M (lymphocyte) - GGB
SR95F (lymphocyte) - GGB
SS86 (lymphocyte, severe combined immunodeficiency disease) - GGB
SS92 (fibroblast, nanism) - GGB
SS95 (lymphocyte, tuberous sclerosis) - GGB
STA88M (lymphocyte) - GGB
SUP-T1 (lymphoma, T cell) - DSMZ
SUP-T1 (pleural effusion, lymphoma, T cell) - ECACC
SUP-T1 (lymphoma, lymphoblastic, T cell) - ICLC
SW 1116 (colon, adenocarcinoma, grade II) - ECACC
SW 13 (adrenal cortex, adenocarcinoma) - ECACC
SW 13 (adrenal cortex, adenocarcinoma) - IZSBS
SW 1463 (rectum, adenocarcinoma) - ECACC
SW 403 (colon, adenocarcinoma, grade II) - ECACC
SW 48 (colon, adenocarcinoma) - ECACC
SW 620 (colon, adenocarcinoma) - ECACC
SW 837 (rectum-anus, adenocarcinoma, grade IV) - ECACC
SW 948 (colon, adenocarcinoma, grade III) - ECACC
SW1353 (bone, chondrosarcoma) - ICLC
SW1417 (colon, adenocarcinoma, grade III) - ICLC
SW48 (colon, adenocarcinoma, grade IV) - ICLC
SW620 (colon, adenocarcinoma) - ICLC
SW620 (colon, adenocarcinoma) - MIILC
SW837 (rectum, adenocarcinoma, grade IV) - ICLC
SW837 (rectum-anus, adenocarcinoma, grade IV) - SPBIC
T 98 G (glioblastoma) - IZSBS
T-1387 (bone marrow, leukemia, acute lymphoblastic) - MWIIW
T-C90 (amnion) - GGB
T-D94 (fibroblast, trisomy 21 / Down syndrome) - GGB
T-F96 (fibroblast, trisomy 21 / Down syndrome) - GGB
T-G88 (amnion, Edwards' syndrome / trisomy 18) - GGB
T-M95a (amnion, trisomy 21 / Down syndrome) - GGB
T-M95f (fibroblast, trisomy 21 / Down syndrome) - GGB
T-P90 (amnion, trisomy 21 / Down syndrome) - GGB
T-P92 (amnion, chromosome aberration) - GGB