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Name Proper Citation Organism Disease Comments Defining Citation Category Sex Synonyms Vendor Catalog Number Cross References Hierarchy Originate from Same Individual ID Record Last Update Mentions Count
GM00017
 
Resource Report
Resource Website
Coriell Cat# GM00017, RRID:CVCL_X222 Homo sapiens (Human) Population: African American. PMID:4780773
PMID:6293786
PMID:6661932
PMID:23665875
Finite cell line Male GM-17, GM-0017, GM0017, GM 17, GM17 Coriell GM00017 CLO:CLO_0025196,
Coriell:GM00017,
Wikidata:Q54835975
CVCL_X222 2026-02-07 08:04:18 0
GM00011
 
Resource Report
Resource Website
RRID:CVCL_7267 Homo sapiens (Human) Population: African American. PMID:694721
PMID:23665875
Finite cell line Male GM0011, GM-11, GM 11, GM11, GM00011A CLO:CLO_0025204,
Coriell:GM00011,
GEO:GSM909336,
GEO:GSM909337,
Wikidata:Q54835971
CVCL_7267 2026-02-07 08:04:18 0
GM00088
 
Resource Report
Resource Website
Coriell Cat# GM00088, RRID:CVCL_X224 Homo sapiens (Human) Turner syndrome Karyotypic information: 46,X,i(X)(p11.21) (PubMed=10377420)., Population: Caucasian. PMID:4780774
PMID:6661932
PMID:10377420
PMID:23665875
Finite cell line Female GM-88, GM-0088, GM0088, GM 88 Coriell GM00088 CLO:CLO_0025156,
Coriell:GM00088,
Wikidata:Q54836029
CVCL_X224 2026-02-07 08:04:29 0
GM00072
 
Resource Report
Resource Website
Coriell Cat# GM00072, RRID:CVCL_V746 Homo sapiens (Human) Wolf-Hirschhorn syndrome Population: Caucasian. PMID:560288
PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Male GM-72, GM-0072, GM 72 Coriell GM00072 CLO:CLO_0025166,
Coriell:GM00072,
Wikidata:Q54836016
CVCL_V746 2026-02-07 08:04:28 0
GM00090
 
Resource Report
Resource Website
RRID:CVCL_H959 Homo sapiens (Human) Nephropathic cystinosis Population: Caucasian. PMID:9792862
PMID:23665875
Finite cell line Male GM0090, GM-90, GM 90, GM00090A, GM0090A CLO:CLO_0025158,
Coriell:GM00090,
Wikidata:Q54836031
CVCL_H959 2026-02-07 08:04:29 0
GM00137
 
Resource Report
Resource Website
Coriell Cat# GM00137, RRID:CVCL_X225 Homo sapiens (Human) Population: Caucasian. PMID:6661932
PMID:23665875
Finite cell line Male GM-137, GM-0137, GM 137, GM00137B Coriell GM00137 CLO:CLO_0025846,
Coriell:GM00137,
Wikidata:Q54836058
CVCL_X225 2026-02-07 08:04:20 0
GM00090
 
Resource Report
Resource Website
Coriell Cat# GM00090, RRID:CVCL_H959 Homo sapiens (Human) Nephropathic cystinosis Population: Caucasian. PMID:9792862
PMID:23665875
Finite cell line Male GM0090, GM-90, GM 90, GM00090A, GM0090A Coriell GM00090 CLO:CLO_0025158,
Coriell:GM00090,
Wikidata:Q54836031
CVCL_H959 2026-02-07 08:04:19 0
GM00088
 
Resource Report
Resource Website
RRID:CVCL_X224 Homo sapiens (Human) Turner syndrome Karyotypic information: 46,X,i(X)(p11.21) (PubMed=10377420)., Population: Caucasian. PMID:4780774
PMID:6661932
PMID:10377420
PMID:23665875
Finite cell line Female GM-88, GM-0088, GM0088, GM 88 CLO:CLO_0025156,
Coriell:GM00088,
Wikidata:Q54836029
CVCL_X224 2026-02-07 08:04:19 0
GM00214
 
Resource Report
Resource Website
Coriell Cat# GM00214, RRID:CVCL_V756 Homo sapiens (Human) Population: Caucasian. PMID:436455
PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Male GM-214, GM-0214, GM0214, GM 214 Coriell GM00214 CLO:CLO_0025664,
Coriell:GM00214,
Wikidata:Q54836094
CVCL_V756 2026-02-07 08:04:21 0
GM00157
 
Resource Report
Resource Website
RRID:CVCL_V753 Homo sapiens (Human) 49,XXXXY syndrome Karyotypic information: 49,XXXXY,t(4;11)(q35;q23).arr(X)x4,(Y)x1 (Coriell=GM00157)., Population: Caucasian. PMID:1132249
PMID:1183238
PMID:6661932
PMID:23665875
Finite cell line Male GM-157, GM-0157, GM 157 CLO:CLO_0025866,
Coriell:GM00157,
Wikidata:Q54836069
CVCL_V753 2026-02-07 08:04:29 0
GM00214
 
Resource Report
Resource Website
RRID:CVCL_V756 Homo sapiens (Human) Population: Caucasian. PMID:436455
PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Male GM-214, GM-0214, GM0214, GM 214 CLO:CLO_0025664,
Coriell:GM00214,
Wikidata:Q54836094
CVCL_V756 2026-02-07 08:04:30 0
GM00343
 
Resource Report
Resource Website
Coriell Cat# GM00343, RRID:CVCL_V766 Homo sapiens (Human) Wolf-Hirschhorn syndrome PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Male GM-343, GM 343 Coriell GM00343 CLO:CLO_0025563,
Coriell:GM00343,
Wikidata:Q54836175
CVCL_V766 2026-02-07 08:04:23 0
GM00343
 
Resource Report
Resource Website
RRID:CVCL_V766 Homo sapiens (Human) Wolf-Hirschhorn syndrome PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Male GM-343, GM 343 CLO:CLO_0025563,
Coriell:GM00343,
Wikidata:Q54836175
CVCL_V766 2026-02-07 08:04:23 0
GM00501
 
Resource Report
Resource Website
Coriell Cat# GM00501, RRID:CVCL_V774 Homo sapiens (Human) Intellectual developmental disorder Population: Caucasian. PMID:1017322
PMID:6661932
PMID:23665875
Finite cell line Male GM-501, GM-0501, GM 501 Coriell GM00501 CLO:CLO_0025946,
Coriell:GM00501,
Wikidata:Q54836267
CVCL_V774 2026-02-07 08:04:33 0
GM00705
 
Resource Report
Resource Website
RRID:CVCL_0P86 Homo sapiens (Human) Karyotypic information: 46,X,t(X;9)(q13.1;p24) (PubMed=10377420)., Population: Caucasian. PMID:113895
PMID:559490
PMID:1056018
PMID:2338345
PMID:8268921
PMID:10377420
PMID:23665875
Finite cell line Female GM-705, GM0705, GM00705A, GM0705A, GMO 705, AnLy CLO:CLO_0028893,
Coriell:GM00705,
Wikidata:Q54836399
CVCL_0P86 2026-02-07 08:04:35 0
GM00705
 
Resource Report
Resource Website
Coriell Cat# GM00705, RRID:CVCL_0P86 Homo sapiens (Human) Karyotypic information: 46,X,t(X;9)(q13.1;p24) (PubMed=10377420)., Population: Caucasian. PMID:113895
PMID:559490
PMID:1056018
PMID:2338345
PMID:8268921
PMID:10377420
PMID:23665875
Finite cell line Female GM-705, GM0705, GM00705A, GM0705A, GMO 705, AnLy Coriell GM00705 CLO:CLO_0028893,
Coriell:GM00705,
Wikidata:Q54836399
CVCL_0P86 2026-02-07 08:04:28 0
GM00692
 
Resource Report
Resource Website
Coriell Cat# GM00692, RRID:CVCL_X235 Homo sapiens (Human) Intellectual developmental disorder Population: Caucasian. PMID:6661932
PMID:23665875
Finite cell line Male GM-692, GM-0692, GM 692 Coriell GM00692 CLO:CLO_0028912,
Coriell:GM00692,
Wikidata:Q54836391
CVCL_X235 2026-02-07 08:04:35 0
GM00735
 
Resource Report
Resource Website
RRID:CVCL_X076 Homo sapiens (Human) Isodicentric chromosome Karyotypic information: 46,X,i(X)(p11) (PubMed=10377420)., Population: Caucasian. PMID:6617268
PMID:6661932
PMID:10377420
PMID:23665875
Finite cell line Female GM-735, GM-0735, GM 735, GM0735 CLO:CLO_0028812,
Coriell:GM00735,
Wikidata:Q54836428
CVCL_X076 2026-02-07 08:04:29 0
GM00782
 
Resource Report
Resource Website
Coriell Cat# GM00782, RRID:CVCL_4E27 Homo sapiens (Human) PMID:23665875 Finite cell line Male GM-782 Coriell GM00782 CLO:CLO_0028841,
Coriell:GM00782,
Wikidata:Q54836455
CVCL_4E27 2026-02-07 08:04:36 0
GM00870
 
Resource Report
Resource Website
RRID:CVCL_V784 Homo sapiens (Human) Intellectual developmental disorder Population: Caucasian. PMID:1017321
PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Female GM-870, GM-0870, GM 870 CLO:CLO_0029601,
Coriell:GM00870,
Wikidata:Q54836493
CVCL_V784 2026-02-07 08:04:31 0

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