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  • References:pmid:23665875 (facet)

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1,669 Results - per page

Show More Columns | Download Top 1000 Results

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
GM20547
 
Resource Report
Resource Website
RRID:CVCL_5R22 Homo sapiens (Human) Isodicentric chromosome PMID:23665875 Transformed cell line Male CLO:CLO_0029707,
Coriell:GM20547,
Wikidata:Q54851103
CVCL_5R22 Cellosaurus 2026-11-07 04:49:12 0
GM20567
 
Resource Report
Resource Website
RRID:CVCL_4E16 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0029680,
Coriell:GM20567,
Wikidata:Q54851111
CVCL_4E16 Cellosaurus 2026-11-07 04:49:12 0
GM20568
 
Resource Report
Resource Website
RRID:CVCL_X437 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM20568,
Wikidata:Q54851112
CVCL_X437 Cellosaurus 2026-11-07 04:49:12 0
GM20571
 
Resource Report
Resource Website
RRID:CVCL_2U61 Homo sapiens (Human) PMID:23665875 Transformed cell line Female CLO:CLO_0029682,
Coriell:GM20571,
Wikidata:Q54851115
CVCL_2U61 Cellosaurus 2026-11-07 04:49:12 0
GM20569
 
Resource Report
Resource Website
Coriell Cat# GM20569, RRID:CVCL_5R30 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM20569 Coriell:GM20569,
Wikidata:Q54851113
CVCL_5R30 Cellosaurus 2026-11-07 04:49:12 0
GM20556
 
Resource Report
Resource Website
RRID:CVCL_5R27 Homo sapiens (Human) Autism spectrum disorder PMID:23665875 Transformed cell line Male CLO:CLO_0029686,
Coriell:GM20556,
Wikidata:Q54851108
CVCL_5R27 Cellosaurus 2026-11-07 04:49:12 0
GM20568
 
Resource Report
Resource Website
Coriell Cat# GM20568, RRID:CVCL_X437 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM20568 Coriell:GM20568,
Wikidata:Q54851112
CVCL_X437 Cellosaurus 2026-11-07 04:49:12 0
GM20738
 
Resource Report
Resource Website
RRID:CVCL_5R32 Homo sapiens (Human) Spondyloepimetaphyseal dysplasia with joint laxity type 2 PMID:23665875 Transformed cell line Male CLO:CLO_0028988,
Coriell:GM20738,
Wikidata:Q54851243
CVCL_5R32 Cellosaurus 2026-11-07 04:49:15 0
GM20916
 
Resource Report
Resource Website
RRID:CVCL_5R33 Homo sapiens (Human) Isodicentric chromosome PMID:23665875 Transformed cell line Female Coriell:GM20916,
Wikidata:Q54851450
CVCL_5R33 Cellosaurus 2026-11-07 04:49:21 0
GM50142
 
Resource Report
Resource Website
RRID:CVCL_5T49 Homo sapiens (Human) PMID:23665875 Transformed cell line Male JL263 CLO:CLO_0014676,
Coriell:GM50142,
Wikidata:Q54854217
CVCL_5T49 Cellosaurus 2026-11-07 04:50:35 0
GM50168
 
Resource Report
Resource Website
RRID:CVCL_5L31 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male JL339 CLO:CLO_0015018,
Coriell:GM50168,
Wikidata:Q54854241
CVCL_5L31 Cellosaurus 2026-11-07 04:50:36 0
GM50152
 
Resource Report
Resource Website
Coriell Cat# GM50152, RRID:CVCL_5L26 Homo sapiens (Human) Deletion 18p syndrome PMID:23665875 Transformed cell line Female JL280 Coriell GM50152 CLO:CLO_0014709,
Coriell:GM50152,
Wikidata:Q54854225
CVCL_5L26 Cellosaurus 2026-11-07 04:50:36 0
GM50150
 
Resource Report
Resource Website
Coriell Cat# GM50150, RRID:CVCL_5T52 Homo sapiens (Human) Holoprosencephaly PMID:23665875 Transformed cell line Female JL278 Coriell GM50150 CLO:CLO_0014715,
Coriell:GM50150,
Wikidata:Q54854224
CVCL_5T52 Cellosaurus 2026-11-07 04:50:36 0
GM50154
 
Resource Report
Resource Website
RRID:CVCL_0G59 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Female JL285 CLO:CLO_0014718,
Coriell:GM50154,
Wikidata:Q54854227
CVCL_0G59 Cellosaurus 2026-11-07 04:50:36 0
GM50116
 
Resource Report
Resource Website
Coriell Cat# GM50116, RRID:CVCL_0F96 Homo sapiens (Human) Deletion 18q syndrome PMID:8488839
PMID:23665875
Transformed cell line Male JL156 Coriell GM50116 CLO:CLO_0014761,
Coriell:GM50116,
Wikidata:Q54854204
CVCL_0F96 Cellosaurus 2026-11-07 04:50:35 0
GM50122
 
Resource Report
Resource Website
Coriell Cat# GM50122, RRID:CVCL_0F92 Homo sapiens (Human) Deletion 18q syndrome PMID:8488839
PMID:23665875
Transformed cell line Male JL184 Coriell GM50122 CLO:CLO_0014752,
Coriell:GM50122,
Wikidata:Q54854208
CVCL_0F92 Cellosaurus 2026-11-07 04:50:35 0
GM50112
 
Resource Report
Resource Website
RRID:CVCL_0G48 Homo sapiens (Human) Cri du chat syndrome PMID:8004090
PMID:23665875
Transformed cell line Female JL137 CLO:CLO_0014757,
Coriell:GM50112,
Wikidata:Q54854200
CVCL_0G48 Cellosaurus 2026-11-07 04:50:35 0
GM50113
 
Resource Report
Resource Website
Coriell Cat# GM50113, RRID:CVCL_0F90 Homo sapiens (Human) Deletion 18q syndrome PMID:8488839
PMID:23665875
Transformed cell line Female JL143 Coriell GM50113 CLO:CLO_0014755,
Coriell:GM50113,
Wikidata:Q54854201
CVCL_0F90 Cellosaurus 2026-11-07 04:50:35 0
GM50147
 
Resource Report
Resource Website
Coriell Cat# GM50147, RRID:CVCL_5T50 Homo sapiens (Human) PMID:23665875 Transformed cell line Female JL273 Coriell GM50147 CLO:CLO_0014683,
Coriell:GM50147,
Wikidata:Q54854221
CVCL_5T50 Cellosaurus 2026-11-07 04:50:36 0
GM50175
 
Resource Report
Resource Website
Coriell Cat# GM50175, RRID:CVCL_5L33 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male JL366 Coriell GM50175 CLO:CLO_0015010,
Coriell:GM50175,
Wikidata:Q54854247
CVCL_5L33 Cellosaurus 2026-11-07 04:50:36 0

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