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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 Record Last Update Mentions Count
GM13031
 
Resource Report
Resource Website
RRID:CVCL_5P72 Homo sapiens (Human) PMID:11687795
PMID:23665875
Transformed cell line Male CLO:CLO_0014030,
Coriell:GM13031,
GEO:GSM808,
Wikidata:Q54846273
CVCL_5P72 2026-02-07 08:08:08 0
GM13031
 
Resource Report
Resource Website
Coriell Cat# GM13031, RRID:CVCL_5P72 Homo sapiens (Human) PMID:11687795
PMID:23665875
Transformed cell line Male Coriell GM13031 CLO:CLO_0014030,
Coriell:GM13031,
GEO:GSM808,
Wikidata:Q54846273
CVCL_5P72 2026-02-07 08:07:59 0
GM13019
 
Resource Report
Resource Website
RRID:CVCL_2N02 Homo sapiens (Human) Turner syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0013986,
Coriell:GM13019,
Wikidata:Q54846265
CVCL_2N02 2026-02-07 08:07:59 0
GM13019
 
Resource Report
Resource Website
Coriell Cat# GM13019, RRID:CVCL_2N02 Homo sapiens (Human) Turner syndrome PMID:23665875 Transformed cell line Female Coriell GM13019 CLO:CLO_0013986,
Coriell:GM13019,
Wikidata:Q54846265
CVCL_2N02 2026-02-07 08:07:59 0
GM13166
 
Resource Report
Resource Website
RRID:CVCL_2Q71 Homo sapiens (Human) Turner syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0013643,
Coriell:GM13166,
Wikidata:Q54846355
CVCL_2Q71 2026-02-07 08:08:11 0
GM13284
 
Resource Report
Resource Website
RRID:CVCL_2U25 Homo sapiens (Human) Population: Caucasian. PMID:23665875 Finite cell line Male CLO:CLO_0013286,
BioSample:SAMN00802254,
Coriell:GM13284,
Wikidata:Q54846420
CVCL_2U25 2026-02-07 08:08:12 0
GM13277
 
Resource Report
Resource Website
Coriell Cat# GM13277, RRID:CVCL_5P73 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM13277 CLO:CLO_0013290,
BioSample:SAMN00802246,
Coriell:GM13277,
Wikidata:Q54846416
CVCL_5P73 2026-02-07 08:08:04 0
GM13419
 
Resource Report
Resource Website
RRID:CVCL_1N85 Homo sapiens (Human) Beckwith-Wiedemann syndrome PMID:23665875 Transformed cell line Male CLO:CLO_0012646,
BioSample:SAMN00802356,
Coriell:GM13419,
Wikidata:Q54846515
CVCL_1N85 2026-02-07 08:08:06 0
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 2026-02-07 08:08:12 0
GM13419
 
Resource Report
Resource Website
Coriell Cat# GM13419, RRID:CVCL_1N85 Homo sapiens (Human) Beckwith-Wiedemann syndrome PMID:23665875 Transformed cell line Male Coriell GM13419 CLO:CLO_0012646,
BioSample:SAMN00802356,
Coriell:GM13419,
Wikidata:Q54846515
CVCL_1N85 2026-02-07 08:08:06 0
GM13410
 
Resource Report
Resource Website
Coriell Cat# GM13410, RRID:CVCL_2U27 Homo sapiens (Human) PMID:23665875 Transformed cell line Sex ambiguous Coriell GM13410 CLO:CLO_0012856,
BioSample:SAMN00802346,
Coriell:GM13410,
Wikidata:Q54846508
CVCL_2U27 2026-02-07 08:08:12 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 2026-02-07 08:08:06 0
GM13330
 
Resource Report
Resource Website
RRID:CVCL_2U26 Homo sapiens (Human) Population: Caucasian. PMID:11687795
PMID:23665875
Finite cell line Male CLO:CLO_0013247,
BioSample:SAMN00802309,
Coriell:GM13330,
GEO:GSM809,
Wikidata:Q54846466
CVCL_2U26 2026-02-07 08:08:12 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 2026-02-07 08:08:07 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 2026-02-07 08:08:07 0
GM13464
 
Resource Report
Resource Website
RRID:CVCL_5P84 Homo sapiens (Human) Williams syndrome Population: Caucasian. PMID:23665875 Transformed cell line Male CLO:CLO_0012187,
BioSample:SAMN00802390,
Coriell:GM13464,
Wikidata:Q54846542
CVCL_5P84 2026-02-07 08:08:07 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 2026-02-07 08:08:07 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 2026-02-07 08:08:13 0
GM13465
 
Resource Report
Resource Website
RRID:CVCL_5P85 Homo sapiens (Human) Williams syndrome Population: Caucasian. PMID:23665875 Transformed cell line Female CLO:CLO_0012195,
BioSample:SAMN00802392,
Coriell:GM13465,
Wikidata:Q54846543
CVCL_5P85 2026-02-07 08:08:07 0
GM13470
 
Resource Report
Resource Website
Coriell Cat# GM13470, RRID:CVCL_5P89 Homo sapiens (Human) Williams syndrome Population: Caucasian. PMID:23665875 Transformed cell line Female Coriell GM13470 CLO:CLO_0012219,
BioSample:SAMN00802400,
Coriell:GM13470,
Wikidata:Q54846550
CVCL_5P89 2026-02-07 08:08:07 0

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