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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
GM07081
 
Resource Report
Resource Website
RRID:CVCL_0Q59 Homo sapiens (Human) Population: Caucasian. PMID:11687795
PMID:23665875
Finite cell line Male CLO:CLO_0036820,
Coriell:GM07081,
GEO:GSM805,
Wikidata:Q54842526
CVCL_0Q59 2026-02-14 08:16:14 0
GM07150
 
Resource Report
Resource Website
RRID:CVCL_2T29 Homo sapiens (Human) PMID:23665875 Finite cell line Female CLO:CLO_0036885,
Coriell:GM07150,
Wikidata:Q54842546
CVCL_2T29 2026-02-14 08:16:14 0
GM07081
 
Resource Report
Resource Website
Coriell Cat# GM07081, RRID:CVCL_0Q59 Homo sapiens (Human) Population: Caucasian. PMID:11687795
PMID:23665875
Finite cell line Male Coriell GM07081 CLO:CLO_0036820,
Coriell:GM07081,
GEO:GSM805,
Wikidata:Q54842526
CVCL_0Q59 2026-02-14 08:16:14 0
GM07151
 
Resource Report
Resource Website
Coriell Cat# GM07151, RRID:CVCL_X048 Homo sapiens (Human) Tetralogy of Fallot Karyotypic information: 46,X,t(X;17)(p11.2;p11.2).arr(1-22,X)x2 (Coriell=GM07151)., Population: Caucasian. PMID:2498246
PMID:23665875
Finite cell line Female GM7151 Coriell GM07151 CLO:CLO_0036891,
Coriell:GM07151,
Wikidata:Q54842547
CVCL_X048 2026-02-14 08:16:15 0
GM07216
 
Resource Report
Resource Website
RRID:CVCL_5N59 Homo sapiens (Human) Holoprosencephaly Population: Caucasian. PMID:23665875 Finite cell line Female CLO:CLO_0036923,
Coriell:GM07216,
Wikidata:Q54842583
CVCL_5N59 2026-02-14 08:16:15 0
GM07215
 
Resource Report
Resource Website
RRID:CVCL_2Y98 Homo sapiens (Human) 22q11.2 deletion syndrome Population: Caucasian. PMID:23665875 Finite cell line Female CLO:CLO_0036922,
Coriell:GM07215,
Wikidata:Q54842582
CVCL_2Y98 2026-02-14 08:16:15 0
GM07312
 
Resource Report
Resource Website
RRID:CVCL_X141 Homo sapiens (Human) Sporadic retinoblastoma PMID:23665875 Transformed cell line Female GM7312, GM07312A CLO:CLO_0035947,
Coriell:GM07312,
Wikidata:Q54842645
CVCL_X141 2026-02-14 08:16:17 0
GM07364
 
Resource Report
Resource Website
RRID:CVCL_4D92 Homo sapiens (Human) Ring chromosome 14 syndrome Population: Caucasian. PMID:23665875 Finite cell line Male CLO:CLO_0016948,
Coriell:GM07364,
Wikidata:Q54842689
CVCL_4D92 2026-02-14 08:16:18 0
GM07427
 
Resource Report
Resource Website
RRID:CVCL_5N63 Homo sapiens (Human) Wilms tumor PMID:2570029
PMID:23665875
Transformed cell line Male GM7427 CLO:CLO_0016881,
Coriell:GM07427,
Wikidata:Q54842748
CVCL_5N63 2026-02-14 08:16:19 0
GM07412
 
Resource Report
Resource Website
Coriell Cat# GM07412, RRID:CVCL_5N62 Homo sapiens (Human) Developmental delay Population: Caucasian. PMID:23665875 Finite cell line Male Coriell GM07412 CLO:CLO_0016914,
Coriell:GM07412,
Wikidata:Q54842725
CVCL_5N62 2026-02-14 08:16:19 0
GM07489
 
Resource Report
Resource Website
RRID:CVCL_F668 Homo sapiens (Human) Hydatidiform mole Population: Southeast Asian; Filipino. PMID:23665875 Cancer cell line Female CLO:CLO_0016483,
Coriell:GM07489,
Wikidata:Q54842785
CVCL_F668 2026-02-14 08:16:20 0
GM12013
 
Resource Report
Resource Website
RRID:CVCL_5P62 Homo sapiens (Human) Population: Caucasian. PMID:23665875 Finite cell line Male CLO:CLO_0020468,
Coriell:GM12013,
Wikidata:Q54845448
CVCL_5P62 2026-02-14 08:17:26 0
GM12025
 
Resource Report
Resource Website
Coriell Cat# GM12025, RRID:CVCL_5L21 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Female Coriell GM12025 CLO:CLO_0020446,
Coriell:GM12025,
Wikidata:Q54845457
CVCL_5L21 2026-02-14 08:17:26 0
GM12013
 
Resource Report
Resource Website
Coriell Cat# GM12013, RRID:CVCL_5P62 Homo sapiens (Human) Population: Caucasian. PMID:23665875 Finite cell line Male Coriell GM12013 CLO:CLO_0020468,
Coriell:GM12013,
Wikidata:Q54845448
CVCL_5P62 2026-02-14 08:17:26 0
GM12025
 
Resource Report
Resource Website
RRID:CVCL_5L21 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0020446,
Coriell:GM12025,
Wikidata:Q54845457
CVCL_5L21 2026-02-14 08:17:26 0
GM12074
 
Resource Report
Resource Website
Coriell Cat# GM12074, RRID:CVCL_5P63 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM12074 CLO:CLO_0020638,
Coriell:GM12074,
Wikidata:Q54845496
CVCL_5P63 2026-02-14 08:17:27 0
GM12074
 
Resource Report
Resource Website
RRID:CVCL_5P63 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0020638,
Coriell:GM12074,
Wikidata:Q54845496
CVCL_5P63 2026-02-14 08:17:27 0
GM12218
 
Resource Report
Resource Website
Coriell Cat# GM12218, RRID:CVCL_5P64 Homo sapiens (Human) PMID:23665875 Finite cell line Female Coriell GM12218 Coriell:GM12218,
Wikidata:Q54845596
CVCL_5P64 2026-02-14 08:17:30 0
GM12134
 
Resource Report
Resource Website
RRID:CVCL_U535 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Male CLO:CLO_0019099,
BioSample:SAMN00801199,
Coriell:GM12134,
Wikidata:Q54845551
CVCL_U535 2026-02-14 08:17:29 0
GM12214
 
Resource Report
Resource Website
RRID:CVCL_1K30 Homo sapiens (Human) Charcot-Marie-Tooth disease type 1A PMID:23665875 Transformed cell line Male CLO:CLO_0019169,
Coriell:GM12214,
Wikidata:Q54845593
CVCL_1K30 2026-02-14 08:17:30 0

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