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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
GM09824
 
Resource Report
Resource Website
Coriell Cat# GM09824, RRID:CVCL_2N13 Homo sapiens (Human) PMID:23665875 Finite cell line Female Coriell GM09824 CLO:CLO_0030660,
Coriell:GM09824,
Wikidata:Q54844078
CVCL_2N13 2026-09-05 10:56:14 0
GM09888
 
Resource Report
Resource Website
RRID:CVCL_5P04 Homo sapiens (Human) Trichorhinophalangeal syndrome type II PMID:23665875 Transformed cell line Female CLO:CLO_0030582,
Coriell:GM09888,
Wikidata:Q54844105
CVCL_5P04 2026-09-05 10:56:15 0
GM09892
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_5P05 Homo sapiens (Human) PMID:23665875 Finite cell line Male CLO:CLO_0030580,
Coriell:GM09892,
Wikidata:Q54844106
CVCL_5P05 2026-09-05 10:56:15 0
GM09892
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM09892, RRID:CVCL_5P05 Homo sapiens (Human) PMID:23665875 Finite cell line Male Coriell GM09892 CLO:CLO_0030580,
Coriell:GM09892,
Wikidata:Q54844106
CVCL_5P05 2026-09-05 10:56:15 0
GM09888
 
Resource Report
Resource Website
Coriell Cat# GM09888, RRID:CVCL_5P04 Homo sapiens (Human) Trichorhinophalangeal syndrome type II PMID:23665875 Transformed cell line Female Coriell GM09888 CLO:CLO_0030582,
Coriell:GM09888,
Wikidata:Q54844105
CVCL_5P04 2026-09-05 10:56:15 0
GM09868
 
Resource Report
Resource Website
RRID:CVCL_F217 Homo sapiens (Human) PMID:23665875 Transformed cell line Female CLO:CLO_0030592,
Coriell:GM09868,
Wikidata:Q54844096
CVCL_F217 2026-09-05 10:56:14 0
GM09868
 
Resource Report
Resource Website
Coriell Cat# GM09868, RRID:CVCL_F217 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM09868 CLO:CLO_0030592,
Coriell:GM09868,
Wikidata:Q54844096
CVCL_F217 2026-09-05 10:56:14 0
GM09988
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_DC01 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM09988,
Wikidata:Q54844145
CVCL_DC01 2026-09-05 10:56:16 0
GM09986
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_IZ54 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell:GM09986,
Wikidata:Q54844143
CVCL_IZ54 2026-09-05 10:56:16 0
GM09986
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM09986, RRID:CVCL_IZ54 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM09986 Coriell:GM09986,
Wikidata:Q54844143
CVCL_IZ54 2026-09-05 10:56:16 0
GM09988
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM09988, RRID:CVCL_DC01 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM09988 Coriell:GM09988,
Wikidata:Q54844145
CVCL_DC01 2026-09-05 10:56:16 0
GM09981
 
Resource Report
Resource Website
RRID:CVCL_5P06 Homo sapiens (Human) Duchenne muscular dystrophy Population: Caucasian., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:21354051
PMID:23665875
Transformed cell line Male CLO:CLO_0029735,
Coriell:GM09981,
Wikidata:Q54844140
CVCL_5P06 2026-09-05 10:56:16 0
GM10006
 
Resource Report
Resource Website
Coriell Cat# GM10006, RRID:CVCL_2T69 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM10006 CLO:CLO_0029789,
BioSample:SAMN00799657,
Coriell:GM10006,
Wikidata:Q54844157
CVCL_2T69 2026-09-05 10:56:17 0
GM10067
 
Resource Report
Resource Website
Coriell Cat# GM10067, RRID:CVCL_2T70 Homo sapiens (Human) Karyotypic information: 46,XY,t(7;13)(7pter->7q34::13q12.3->13qter;13pter->13q12.3::7q34->7qter) (Coriell=GM10067)., Population: Caucasian. PMID:23665875 Transformed cell line Male Coriell GM10067 CLO:CLO_0029847,
BioSample:SAMN00799681,
Coriell:GM10067,
Wikidata:Q54844195
CVCL_2T70 2026-09-05 10:56:17 0
GM10064
 
Resource Report
Resource Website
Coriell Cat# GM10064, RRID:CVCL_5P10 Homo sapiens (Human) Holoprosencephaly Karyotypic information: 46,XX,der(7)(7pter->7q34::13q12.3->13qter)pat (Coriell=GM10064)., Population: Caucasian. PMID:23665875 Finite cell line Female Coriell GM10064 CLO:CLO_0029841,
BioSample:SAMN00799679,
Coriell:GM10064,
Wikidata:Q54844194
CVCL_5P10 2026-09-05 10:56:17 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 2026-09-05 10:55:42 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 2026-09-05 10:55:42 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 2026-09-05 10:55:43 0
GM07773
 
Resource Report
Resource Website
RRID:CVCL_5N69 Homo sapiens (Human) Chronic granulomatous disease PMID:23665875 Transformed cell line Female CLO:CLO_0016358,
Coriell:GM07773,
Wikidata:Q54842898
CVCL_5N69 2026-09-05 10:55:45 0
GM07773
 
Resource Report
Resource Website
Coriell Cat# GM07773, RRID:CVCL_5N69 Homo sapiens (Human) Chronic granulomatous disease PMID:23665875 Transformed cell line Female Coriell GM07773 CLO:CLO_0016358,
Coriell:GM07773,
Wikidata:Q54842898
CVCL_5N69 2026-09-05 10:55:45 0

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