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  • References:pmid:23665875 (facet)

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1,669 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 Authority Record Last Update Mentions Count
GM21878
 
Resource Report
Resource Website
Coriell Cat# GM21878, RRID:CVCL_5R41 Homo sapiens (Human) PMID:23665875 Finite cell line Female Coriell GM21878 Coriell:GM21878,
Wikidata:Q54852196
CVCL_5R41 Cellosaurus 2026-09-19 05:32:07 0
GM21871
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_5R39 Homo sapiens (Human) Roberts-SC phocomelia syndrome PMID:23665875 Transformed cell line Female Coriell:GM21871,
Wikidata:Q54852191
CVCL_5R39 Cellosaurus 2026-09-19 05:32:07 0
GM21886
 
Resource Report
Resource Website
Coriell Cat# GM21886, RRID:CVCL_5R45 Homo sapiens (Human) Supernumerary circular chromosome PMID:23665875 Transformed cell line Male Coriell GM21886 Coriell:GM21886,
Wikidata:Q54852208
CVCL_5R45 Cellosaurus 2026-09-19 05:32:07 0
GM21887
 
Resource Report
Resource Website
RRID:CVCL_5R46 Homo sapiens (Human) Angelman syndrome PMID:23665875 Transformed cell line Female Coriell:GM21887,
Wikidata:Q54852209
CVCL_5R46 Cellosaurus 2026-09-19 05:32:07 0
GM21883
 
Resource Report
Resource Website
Coriell Cat# GM21883, RRID:CVCL_5R42 Homo sapiens (Human) Supernumerary circular chromosome PMID:23665875 Transformed cell line Male Coriell GM21883 Coriell:GM21883,
Wikidata:Q54852205
CVCL_5R42 Cellosaurus 2026-09-19 05:32:07 0
GM22031
 
Resource Report
Resource Website
Coriell Cat# GM22031, RRID:CVCL_5R49 Homo sapiens (Human) Azoospermia PMID:23665875 Transformed cell line Male Coriell GM22031 Coriell:GM22031,
Wikidata:Q54852309
CVCL_5R49 Cellosaurus 2026-09-19 05:32:09 0
GM22032
 
Resource Report
Resource Website
RRID:CVCL_5R50 Homo sapiens (Human) Azoospermia PMID:23665875 Transformed cell line Male CLO:CLO_0014824,
Coriell:GM22032,
Wikidata:Q54852310
CVCL_5R50 Cellosaurus 2026-09-19 05:32:09 0
GM22122
 
Resource Report
Resource Website
RRID:CVCL_5R53 Homo sapiens (Human) PMID:23665875 Finite cell line Male Coriell:GM22122,
Wikidata:Q54852360
CVCL_5R53 Cellosaurus 2026-09-19 05:32:10 0
GM22439
 
Resource Report
Resource Website
Coriell Cat# GM22439, RRID:CVCL_5M61 Homo sapiens (Human) Jacobsen syndrome PMID:23665875 Transformed cell line Female Coriell GM22439 Coriell:GM22439,
Wikidata:Q54852567
CVCL_5M61 Cellosaurus 2026-09-19 05:32:15 0
GM22421
 
Resource Report
Resource Website
RRID:CVCL_5M60 Homo sapiens (Human) Jacobsen syndrome PMID:23665875 Transformed cell line Male Coriell:GM22421,
Wikidata:Q54852566
CVCL_5M60 Cellosaurus 2026-09-19 05:32:15 0
GM22364
 
Resource Report
Resource Website
RRID:CVCL_5R61 Homo sapiens (Human) Chromosome 15q11-q13 duplication syndrome PMID:23495136
PMID:23665875
Transformed cell line Male 801-005 LCL Coriell:GM22364,
Wikidata:Q54852542
CVCL_5R61 Cellosaurus 2026-09-19 05:32:14 0
GM22569
 
Resource Report
Resource Website
Coriell Cat# GM22569, RRID:CVCL_5R82 Homo sapiens (Human) 1p36 deletion syndrome PMID:23665875 Transformed cell line Female Coriell GM22569 Coriell:GM22569,
Wikidata:Q54852629
CVCL_5R82 Cellosaurus 2026-09-19 05:32:16 0
GM22601
 
Resource Report
Resource Website
RRID:CVCL_V824 Homo sapiens (Human) Wolf-Hirschhorn syndrome PMID:23665875 Transformed cell line Male Coriell:GM22601,
Wikidata:Q54852650
CVCL_V824 Cellosaurus 2026-09-19 05:32:17 0
GM22626
 
Resource Report
Resource Website
RRID:CVCL_1K39 Homo sapiens (Human) Potocki-Shaffer syndrome PMID:23665875 Transformed cell line Male Coriell:GM22626,
Wikidata:Q54852667
CVCL_1K39 Cellosaurus 2026-09-19 05:32:17 0
GM22634
 
Resource Report
Resource Website
Coriell Cat# GM22634, RRID:CVCL_5R93 Homo sapiens (Human) Primary open angle glaucoma Population: Caucasian. PMID:23665875 Transformed cell line Female Coriell GM22634 Coriell:GM22634,
Wikidata:Q54852677
CVCL_5R93 Cellosaurus 2026-09-19 05:32:18 0
GM22569
 
Resource Report
Resource Website
RRID:CVCL_5R82 Homo sapiens (Human) 1p36 deletion syndrome PMID:23665875 Transformed cell line Female Coriell:GM22569,
Wikidata:Q54852629
CVCL_5R82 Cellosaurus 2026-09-19 05:32:16 0
GM22623
 
Resource Report
Resource Website
RRID:CVCL_1K36 Homo sapiens (Human) Karyotypic information: 46,XX,ins(13;11)(q14.1;p11.2p12).ish ins(13;11)(q14.1;p11.2p12)(wcp11+).arr(1-22,X)x2 (Coriell=GM22623). PMID:23665875 Transformed cell line Female Coriell:GM22623,
Wikidata:Q54852664
CVCL_1K36 Cellosaurus 2026-09-19 05:32:17 0
GM22634
 
Resource Report
Resource Website
RRID:CVCL_5R93 Homo sapiens (Human) Primary open angle glaucoma Population: Caucasian. PMID:23665875 Transformed cell line Female Coriell:GM22634,
Wikidata:Q54852677
CVCL_5R93 Cellosaurus 2026-09-19 05:32:18 0
GM22593
 
Resource Report
Resource Website
RRID:CVCL_5R86 Homo sapiens (Human) Autism spectrum disorder PMID:23495136
PMID:23665875
Transformed cell line Female 801-009 LCL Coriell:GM22593,
Wikidata:Q54852642
CVCL_5R86 Cellosaurus 2026-09-19 05:32:17 0
GM22630
 
Resource Report
Resource Website
RRID:CVCL_1K43 Homo sapiens (Human) Potocki-Shaffer syndrome PMID:23665875 Transformed cell line Female Coriell:GM22630,
Wikidata:Q54852671
CVCL_1K43 Cellosaurus 2026-09-19 05:32:18 0

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