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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
GM20434
 
Resource Report
Resource Website
RRID:CVCL_5R16 Homo sapiens (Human) Azoospermia PMID:23665875 Transformed cell line Male CLO:CLO_0029513,
Coriell:GM20434,
Wikidata:Q54851024
CVCL_5R16 Cellosaurus 2026-10-24 05:31:32 0
GM20501
 
Resource Report
Resource Website
Coriell Cat# GM20501, RRID:CVCL_5R19 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM20501 CLO:CLO_0029528,
Coriell:GM20501,
Wikidata:Q54851048
CVCL_5R19 Cellosaurus 2026-10-24 05:31:33 0
GM20548
 
Resource Report
Resource Website
Coriell Cat# GM20548, RRID:CVCL_5R23 Homo sapiens (Human) Isodicentric chromosome PMID:23665875 Transformed cell line Sex ambiguous Coriell GM20548 CLO:CLO_0029687,
Coriell:GM20548,
Wikidata:Q54851104
CVCL_5R23 Cellosaurus 2026-10-24 05:31:34 0
GM20569
 
Resource Report
Resource Website
RRID:CVCL_5R30 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM20569,
Wikidata:Q54851113
CVCL_5R30 Cellosaurus 2026-10-24 05:31:34 0
GM20567
 
Resource Report
Resource Website
Coriell Cat# GM20567, RRID:CVCL_4E16 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM20567 CLO:CLO_0029680,
Coriell:GM20567,
Wikidata:Q54851111
CVCL_4E16 Cellosaurus 2026-10-24 05:31:34 0
GM20571
 
Resource Report
Resource Website
Coriell Cat# GM20571, RRID:CVCL_2U61 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM20571 CLO:CLO_0029682,
Coriell:GM20571,
Wikidata:Q54851115
CVCL_2U61 Cellosaurus 2026-10-24 05:31:34 0
GM20562
 
Resource Report
Resource Website
Coriell Cat# GM20562, RRID:CVCL_5R29 Homo sapiens (Human) Autism spectrum disorder Karyotypic information: 47,XX,+idic(15)(pter>q13::q13>pter).ish idic(15)(D15Z1++,D15S11++,GABRB3++) (Coriell=GM20562)., Population: Caucasian. PMID:23665875
PMID:39059105
Transformed cell line Female Coriell GM20562 CLO:CLO_0029685,
Coriell:GM20562,
Wikidata:Q54851110
CVCL_5R29 Cellosaurus 2026-10-24 05:31:34 0
GM20562
 
Resource Report
Resource Website
RRID:CVCL_5R29 Homo sapiens (Human) Autism spectrum disorder Karyotypic information: 47,XX,+idic(15)(pter>q13::q13>pter).ish idic(15)(D15Z1++,D15S11++,GABRB3++) (Coriell=GM20562)., Population: Caucasian. PMID:23665875
PMID:39059105
Transformed cell line Female CLO:CLO_0029685,
Coriell:GM20562,
Wikidata:Q54851110
CVCL_5R29 Cellosaurus 2026-10-24 05:31:34 0
GM20547
 
Resource Report
Resource Website
Coriell Cat# GM20547, RRID:CVCL_5R22 Homo sapiens (Human) Isodicentric chromosome PMID:23665875 Transformed cell line Male Coriell GM20547 CLO:CLO_0029707,
Coriell:GM20547,
Wikidata:Q54851103
CVCL_5R22 Cellosaurus 2026-10-24 05:31:34 0
GM20550
 
Resource Report
Resource Website
Coriell Cat# GM20550, RRID:CVCL_5R24 Homo sapiens (Human) Autism spectrum disorder PMID:23665875 Transformed cell line Male Coriell GM20550 CLO:CLO_0029688,
Coriell:GM20550,
Wikidata:Q54851105
CVCL_5R24 Cellosaurus 2026-10-24 05:31:34 0
GM20550
 
Resource Report
Resource Website
RRID:CVCL_5R24 Homo sapiens (Human) Autism spectrum disorder PMID:23665875 Transformed cell line Male CLO:CLO_0029688,
Coriell:GM20550,
Wikidata:Q54851105
CVCL_5R24 Cellosaurus 2026-10-24 05:31:34 0
GM20545
 
Resource Report
Resource Website
RRID:CVCL_5R20 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0029703,
Coriell:GM20545,
Wikidata:Q54851101
CVCL_5R20 Cellosaurus 2026-10-24 05:31:34 0
GM20570
 
Resource Report
Resource Website
Coriell Cat# GM20570, RRID:CVCL_5R31 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM20570 CLO:CLO_0029679,
Coriell:GM20570,
Wikidata:Q54851114
CVCL_5R31 Cellosaurus 2026-10-24 05:31:34 0
GM20570
 
Resource Report
Resource Website
RRID:CVCL_5R31 Homo sapiens (Human) PMID:23665875 Transformed cell line Female CLO:CLO_0029679,
Coriell:GM20570,
Wikidata:Q54851114
CVCL_5R31 Cellosaurus 2026-10-24 05:31:34 0
GM20548
 
Resource Report
Resource Website
RRID:CVCL_5R23 Homo sapiens (Human) Isodicentric chromosome PMID:23665875 Transformed cell line Sex ambiguous CLO:CLO_0029687,
Coriell:GM20548,
Wikidata:Q54851104
CVCL_5R23 Cellosaurus 2026-10-24 05:31:34 0
GM20556
 
Resource Report
Resource Website
Coriell Cat# GM20556, RRID:CVCL_5R27 Homo sapiens (Human) Autism spectrum disorder PMID:23665875 Transformed cell line Male Coriell GM20556 CLO:CLO_0029686,
Coriell:GM20556,
Wikidata:Q54851108
CVCL_5R27 Cellosaurus 2026-10-24 05:31:34 0
GM20743
 
Resource Report
Resource Website
Coriell Cat# GM20743, RRID:CVCL_5K23 Homo sapiens (Human) Smith-Magenis syndrome PMID:23665875 Transformed cell line Male Coriell GM20743 CLO:CLO_0029027,
Coriell:GM20743,
Wikidata:Q54851246
CVCL_5K23 Cellosaurus 2026-10-24 05:31:37 0
GM20738
 
Resource Report
Resource Website
Coriell Cat# GM20738, RRID:CVCL_5R32 Homo sapiens (Human) Spondyloepimetaphyseal dysplasia with joint laxity type 2 PMID:23665875 Transformed cell line Male Coriell GM20738 CLO:CLO_0028988,
Coriell:GM20738,
Wikidata:Q54851243
CVCL_5R32 Cellosaurus 2026-10-24 05:31:37 0
GM20743
 
Resource Report
Resource Website
RRID:CVCL_5K23 Homo sapiens (Human) Smith-Magenis syndrome PMID:23665875 Transformed cell line Male CLO:CLO_0029027,
Coriell:GM20743,
Wikidata:Q54851246
CVCL_5K23 Cellosaurus 2026-10-24 05:31:37 0
GM15913
 
Resource Report
Resource Website
Coriell Cat# GM15913, RRID:CVCL_5Q61 Homo sapiens (Human) Waardenburg syndrome type 4 Population: African American. PMID:23665875 Transformed cell line Female Coriell GM15913 Coriell:GM15913,
Wikidata:Q54848276
CVCL_5Q61 Cellosaurus 2026-10-24 05:30:43 0

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