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95,747 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
GM13324
 
Resource Report
Resource Website
Coriell Cat# GM13324, RRID:CVCL_2N05 Homo sapiens (Human) Turner syndrome Donor information: Established from monozygotic twin of GM13323 (Cellosaurus=CVCL_2N04). PMID:23665875 Transformed cell line Female Coriell GM13324 CLO:CLO_0013274,
Coriell:GM13324,
Wikidata:Q54846461
CVCL_2N05 2026-08-08 05:02:28 0
GM13356
 
Resource Report
Resource Website
RRID:CVCL_0I46 Homo sapiens (Human) Part of: CEPH/Venezuelan pedigree cell line collection. Transformed cell line Female CLO:CLO_0012842,
Coriell:GM13356,
Wikidata:Q54846480
CVCL_0I46 2026-08-08 05:02:29 0
GM13313
 
Resource Report
Resource Website
Coriell Cat# GM13313, RRID:CVCL_4F09 Homo sapiens (Human) Ellis-Van Creveld syndrome Population: Caucasian; Amish. Transformed cell line Female Coriell GM13313 CLO:CLO_0013217,
BioSample:SAMN00802291,
Coriell:GM13313,
Wikidata:Q54846453
CVCL_4F09 2026-08-08 05:02:28 0
GM13347
 
Resource Report
Resource Website
Coriell Cat# GM13347, RRID:CVCL_4W22 Homo sapiens (Human) Rubinstein-Taybi syndrome Transformed cell line Female Coriell GM13347 CLO:CLO_0012891,
BioSample:SAMN00802322,
Coriell:GM13347,
Wikidata:Q54846476
CVCL_4W22 2026-08-08 05:02:29 0
GM13415
 
Resource Report
Resource Website
Coriell Cat# GM13415, RRID:CVCL_1N83 Homo sapiens (Human) Beckwith-Wiedemann syndrome PMID:23665875 Transformed cell line Female Coriell GM13415 CLO:CLO_0012653,
BioSample:SAMN00802350,
Coriell:GM13415,
Wikidata:Q54846512
CVCL_1N83 2026-08-08 05:02:29 0
GM13352
 
Resource Report
Resource Website
RRID:CVCL_1K74 Homo sapiens (Human) Glycogen storage disease type II Population: Indian. Finite cell line Female CLO:CLO_0012903,
BioSample:SAMN00802326,
Coriell:GM13352,
Wikidata:Q54846478
CVCL_1K74 2026-08-08 05:02:29 0
GM13363
 
Resource Report
Resource Website
RRID:CVCL_Y602 Homo sapiens (Human) Charcot-Marie-Tooth disease type 1B Transformed cell line Female CLO:CLO_0012844,
BioSample:SAMN00802332,
Coriell:GM13363,
Wikidata:Q54846482
CVCL_Y602 2026-08-08 05:02:29 0
GM13439
 
Resource Report
Resource Website
RRID:CVCL_CX12 Homo sapiens (Human) Glycine encephalopathy Population: Jordanian. Transformed cell line Female CLO:CLO_0012666,
BioSample:SAMN00802376,
Coriell:GM13439,
Wikidata:Q54846529
CVCL_CX12 2026-08-08 05:02:30 0
GM13315
 
Resource Report
Resource Website
Coriell Cat# GM13315, RRID:CVCL_4F11 Homo sapiens (Human) Ellis-Van Creveld syndrome Population: Caucasian; Amish. Transformed cell line Female Coriell GM13315 CLO:CLO_0013219,
BioSample:SAMN00802295,
Coriell:GM13315,
Wikidata:Q54846456
CVCL_4F11 2026-08-08 05:02:28 0
GM13527
 
Resource Report
Resource Website
RRID:CVCL_1K80 Homo sapiens (Human) Glycogen storage disease type II Population: Caucasian. Transformed cell line Female CLO:CLO_0012400,
BioSample:SAMN00802448,
Coriell:GM13527,
Wikidata:Q54846614
CVCL_1K80 2026-08-08 05:02:31 0
GM13471
 
Resource Report
Resource Website
Coriell Cat# GM13471, RRID:CVCL_5P90 Homo sapiens (Human) Williams syndrome Population: Caucasian. Transformed cell line Female Coriell GM13471 CLO:CLO_0012214,
BioSample:SAMN00802402,
Coriell:GM13471,
Wikidata:Q54846558
CVCL_5P90 2026-08-08 05:02:30 0
GM13465
 
Resource Report
Resource Website
Coriell Cat# GM13465, RRID:CVCL_5P85 Homo sapiens (Human) Williams syndrome Population: Caucasian. PMID:23665875 Transformed cell line Female Coriell GM13465 CLO:CLO_0012195,
BioSample:SAMN00802392,
Coriell:GM13465,
Wikidata:Q54846543
CVCL_5P85 2026-08-08 05:02:30 0
GM13478
 
Resource Report
Resource Website
Coriell Cat# GM13478, RRID:CVCL_5P96 Homo sapiens (Human) Williams syndrome Population: Caucasian. PMID:23665875 Transformed cell line Female Coriell GM13478 CLO:CLO_0012250,
BioSample:SAMN00802416,
Coriell:GM13478,
Wikidata:Q54846565
CVCL_5P96 2026-08-08 05:02:30 0
GM13523
 
Resource Report
Resource Website
Coriell Cat# GM13523, RRID:CVCL_4I85 Homo sapiens (Human) Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection. Transformed cell line Female Coriell GM13523 CLO:CLO_0012406,
Coriell:GM13523,
Wikidata:Q54846609
CVCL_4I85 2026-08-08 05:02:31 0
GM13488
 
Resource Report
Resource Website
RRID:CVCL_5Q05 Homo sapiens (Human) Williams syndrome Population: Caucasian. Transformed cell line Female CLO:CLO_0012337,
BioSample:SAMN00802436,
Coriell:GM13488,
Wikidata:Q54846577
CVCL_5Q05 2026-08-08 05:02:30 0
GM13503
 
Resource Report
Resource Website
RRID:CVCL_1J70 Homo sapiens (Human) Huntington's disease Transformed cell line Female CLO:CLO_0012363,
Coriell:GM13503,
Wikidata:Q54846589
CVCL_1J70 2026-08-08 05:02:31 0
GM13527
 
Resource Report
Resource Website
Coriell Cat# GM13527, RRID:CVCL_1K80 Homo sapiens (Human) Glycogen storage disease type II Population: Caucasian. Transformed cell line Female Coriell GM13527 CLO:CLO_0012400,
BioSample:SAMN00802448,
Coriell:GM13527,
Wikidata:Q54846614
CVCL_1K80 2026-08-08 05:02:32 0
GM13489
 
Resource Report
Resource Website
Coriell Cat# GM13489, RRID:CVCL_5Q06 Homo sapiens (Human) Williams syndrome Population: Caucasian. Transformed cell line Female Coriell GM13489 CLO:CLO_0012307,
BioSample:SAMN00802438,
Coriell:GM13489,
Wikidata:Q54846578
CVCL_5Q06 2026-08-08 05:02:31 0
GM13482
 
Resource Report
Resource Website
Coriell Cat# GM13482, RRID:CVCL_5Q00 Homo sapiens (Human) Williams syndrome Population: Caucasian. PMID:23665875 Transformed cell line Female Coriell GM13482 CLO:CLO_0012259,
BioSample:SAMN00802424,
Coriell:GM13482,
Wikidata:Q54846569
CVCL_5Q00 2026-08-08 05:02:31 0
GM13482
 
Resource Report
Resource Website
RRID:CVCL_5Q00 Homo sapiens (Human) Williams syndrome Population: Caucasian. PMID:23665875 Transformed cell line Female CLO:CLO_0012259,
BioSample:SAMN00802424,
Coriell:GM13482,
Wikidata:Q54846569
CVCL_5Q00 2026-08-08 05:02:30 0

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