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256,031 Results - per page

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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
GM04937
 
Resource Report
Resource Website
RRID:CVCL_8A06 Homo sapiens (Human) Tourette syndrome Population: Caucasian. Finite cell line Female CLO:CLO_0025577,
Coriell:GM04937,
Wikidata:Q54838774
CVCL_8A06 2026-08-08 05:00:20 0
GM04928
 
Resource Report
Resource Website
Coriell Cat# GM04928, RRID:CVCL_V478 Homo sapiens (Human) Down syndrome PMID:6661932
PMID:8643543
Finite cell line Male GM 4928, GM04928A, GM 4928A Coriell GM04928 CLO:CLO_0025601,
Coriell:GM04928,
Wikidata:Q54838765
CVCL_V478 2026-08-08 05:00:20 0
GM04863
 
Resource Report
Resource Website
RRID:CVCL_4N45 Homo sapiens (Human) Population: Jewish; Ashkenazi. PMID:19815695 Finite cell line Male GM 4863 CLO:CLO_0025793,
Coriell:GM04863,
Wikidata:Q54838732
CVCL_4N45 2026-08-08 05:00:19 0
GM04932
 
Resource Report
Resource Website
Coriell Cat# GM04932, RRID:CVCL_N034 Homo sapiens (Human) Adrenoleukodystrophy Population: Pacific., Part of: Human variation panel. Finite cell line Male GM17386 Coriell GM04932 CLO:CLO_0012164,
CLO:CLO_0025574,
Coriell:GM04932,
Coriell:GM17386,
Wikidata:Q54838770
CVCL_N034 2026-08-08 05:00:20 0
GM04849
 
Resource Report
Resource Website
RRID:CVCL_1I57 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Female CLO:CLO_0018176,
Coriell:GM04849,
Wikidata:Q54838718
CVCL_1I57 2026-08-08 05:00:19 0
GM04894
 
Resource Report
Resource Website
RRID:CVCL_1I74 Homo sapiens (Human) Huntington's disease Population: Caucasian. Transformed cell line Male CLO:CLO_0025768,
Coriell:GM04894,
Wikidata:Q54838744
CVCL_1I74 2026-08-08 05:00:20 0
GM04921
 
Resource Report
Resource Website
Coriell Cat# GM04921, RRID:CVCL_2T09 Homo sapiens (Human) Karyotypic information: 46,XX,t(4;8)(4qter->4p15::8p22->8pter;8qter->8p22::4p15->4pter) (Coriell=GM04921)., Population: Caucasian. Finite cell line Female Coriell GM04921 CLO:CLO_0025602,
Coriell:GM04921,
Wikidata:Q54838762
CVCL_2T09 2026-08-08 05:00:20 0
GM04866
 
Resource Report
Resource Website
RRID:CVCL_1I70 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Male GM04866A, GM04866B CLO:CLO_0025788,
Coriell:GM04866,
Wikidata:Q54838735
CVCL_1I70 2026-08-08 05:00:20 0
GM04902
 
Resource Report
Resource Website
RRID:CVCL_JL91 Homo sapiens (Human) Glucocorticoid resistance Population: Caucasian; Dutch. Finite cell line Male CLO:CLO_0025592,
Coriell:GM04902,
Wikidata:Q54838752
CVCL_JL91 2026-08-08 05:00:20 0
GM04862
 
Resource Report
Resource Website
Coriell Cat# GM04862, RRID:CVCL_2T07 Homo sapiens (Human) Karyotypic information: 46,XX,t(7;21)(7pter->7q36::21q21->21qter;21pter->21q21::7q36->7qter) (Coriell=GM04862)., Population: Caucasian. Finite cell line Female Coriell GM04862 CLO:CLO_0025794,
Coriell:GM04862,
Wikidata:Q54838731
CVCL_2T07 2026-08-08 05:00:20 0
GM04932
 
Resource Report
Resource Website
Coriell Cat# GM17386, RRID:CVCL_N034 Homo sapiens (Human) Adrenoleukodystrophy Population: Pacific., Part of: Human variation panel. Finite cell line Male GM17386 Coriell GM17386 CLO:CLO_0012164,
CLO:CLO_0025574,
Coriell:GM04932,
Coriell:GM17386,
Wikidata:Q54838770
CVCL_N034 2026-08-08 05:00:21 0
GM04847
 
Resource Report
Resource Website
Coriell Cat# GM04847, RRID:CVCL_1I56 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Male Coriell GM04847 CLO:CLO_0018179,
Coriell:GM04847,
Wikidata:Q54838717
CVCL_1I56 2026-08-08 05:00:19 0
GM04857
 
Resource Report
Resource Website
RRID:CVCL_1I63 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. PMID:25928884
PMID:30256717
Finite cell line Female CLO:CLO_0018184,
Coriell:GM04857,
Wikidata:Q54838724
CVCL_1I63 2026-08-08 05:00:19 0
GM04937
 
Resource Report
Resource Website
Coriell Cat# GM04937, RRID:CVCL_8A06 Homo sapiens (Human) Tourette syndrome Population: Caucasian. Finite cell line Female Coriell GM04937 CLO:CLO_0025577,
Coriell:GM04937,
Wikidata:Q54838774
CVCL_8A06 2026-08-08 05:00:22 0
GM04865
 
Resource Report
Resource Website
Coriell Cat# GM04865, RRID:CVCL_1I69 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Male Coriell GM04865 CLO:CLO_0025789,
Coriell:GM04865,
Wikidata:Q54838734
CVCL_1I69 2026-08-08 05:00:19 0
GM04911
 
Resource Report
Resource Website
Coriell Cat# GM04911, RRID:CVCL_9R81 Homo sapiens (Human) Kniest dysplasia Population: Caucasian. Finite cell line Male Coriell GM04911 CLO:CLO_0025590,
Coriell:GM04911,
Wikidata:Q54838756
CVCL_9R81 2026-08-08 05:00:20 0
GM04913
 
Resource Report
Resource Website
Coriell Cat# GM04913, RRID:CVCL_2Z52 Homo sapiens (Human) Krabbe disease Population: Caucasian; Greek. Finite cell line Sex unspecified Coriell GM04913 CLO:CLO_0025606,
Coriell:GM04913,
Wikidata:Q54838758
CVCL_2Z52 2026-08-08 05:00:21 0
GM04910
 
Resource Report
Resource Website
RRID:CVCL_VH33 Homo sapiens (Human) Bannayan syndrome Population: Caucasian; French/German. Finite cell line Female CLO:CLO_0025589,
Coriell:GM04910,
Wikidata:Q54838755
CVCL_VH33 2026-08-08 05:00:20 0
GM04911
 
Resource Report
Resource Website
RRID:CVCL_9R81 Homo sapiens (Human) Kniest dysplasia Population: Caucasian. Finite cell line Male CLO:CLO_0025590,
Coriell:GM04911,
Wikidata:Q54838756
CVCL_9R81 2026-08-08 05:00:20 0
GM04847
 
Resource Report
Resource Website
RRID:CVCL_1I56 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Male CLO:CLO_0018179,
Coriell:GM04847,
Wikidata:Q54838717
CVCL_1I56 2026-08-08 05:00:20 0

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