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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
GM09025
 
Resource Report
Resource Website
RRID:CVCL_4D94 Homo sapiens (Human) Supernumerary circular chromosome PMID:23665875 Transformed cell line Male CLO:CLO_0010836,
BioSample:SAMN00798441,
Coriell:GM09025,
Wikidata:Q54843508
CVCL_4D94 2026-09-05 10:56:00 0
GM09026
 
Resource Report
Resource Website
Coriell Cat# GM09026, RRID:CVCL_0L61 Homo sapiens (Human) Population: African American. PMID:23665875 Finite cell line Male Coriell GM09026 CLO:CLO_0010837,
BioSample:SAMN00798443,
Coriell:GM09026,
Wikidata:Q54843509
cvcl_0l60 CVCL_0L61 2026-09-05 10:56:00 0
GM09024
 
Resource Report
Resource Website
Coriell Cat# GM09024, RRID:CVCL_0L59 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Male Coriell GM09024 CLO:CLO_0010734,
BioSample:SAMN00798439,
Coriell:GM09024,
Wikidata:Q54843507
CVCL_0L59 2026-09-05 10:56:00 0
GM09101
 
Resource Report
Resource Website
Coriell Cat# GM09101, RRID:CVCL_5N94 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM09101 CLO:CLO_0010655,
BioSample:SAMN00798547,
Coriell:GM09101,
Wikidata:Q54843585
CVCL_5N94 2026-09-05 10:56:02 0
GM09189
 
Resource Report
Resource Website
Coriell Cat# GM09189, RRID:CVCL_5N97 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Female Coriell GM09189 CLO:CLO_0010631,
BioSample:SAMN00798575,
Coriell:GM09189,
Wikidata:Q54843603
CVCL_5N97 2026-09-05 10:56:02 0
GM09216
 
Resource Report
Resource Website
Coriell Cat# GM09216, RRID:CVCL_V823 Homo sapiens (Human) Population: African American. PMID:23665875 Transformed cell line Male Coriell GM09216 CLO:CLO_0010685,
BioSample:SAMN00798587,
Coriell:GM09216,
Wikidata:Q54843618
CVCL_V823 2026-09-05 10:56:03 0
GM09189
 
Resource Report
Resource Website
RRID:CVCL_5N97 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0010631,
BioSample:SAMN00798575,
Coriell:GM09189,
Wikidata:Q54843603
CVCL_5N97 2026-09-05 10:56:02 0
GM09101
 
Resource Report
Resource Website
RRID:CVCL_5N94 Homo sapiens (Human) PMID:23665875 Transformed cell line Female CLO:CLO_0010655,
BioSample:SAMN00798547,
Coriell:GM09101,
Wikidata:Q54843585
CVCL_5N94 2026-09-05 10:56:02 0
GM09285
 
Resource Report
Resource Website
RRID:CVCL_2T62 Homo sapiens (Human) Population: Caucasian. PMID:23665875 Finite cell line Female CLO:CLO_0012057,
Coriell:GM09285,
Wikidata:Q54843646
CVCL_2T62 2026-09-05 10:56:04 0
GM04626
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM04626, RRID:CVCL_X310 Homo sapiens (Human) PMID:6661932
PMID:21177337
PMID:23665875
Finite cell line Female GM 4626 Coriell GM04626 CLO:CLO_0018940,
Coriell:GM04626,
GEO:GSM608319,
GEO:GSM608320,
Wikidata:Q54838608
CVCL_X310 2026-09-05 10:55:04 1
GM04626
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_X310 Homo sapiens (Human) PMID:6661932
PMID:21177337
PMID:23665875
Finite cell line Female GM 4626 CLO:CLO_0018940,
Coriell:GM04626,
GEO:GSM608319,
GEO:GSM608320,
Wikidata:Q54838608
CVCL_X310 2026-09-05 10:55:04 1
GM04619
 
Resource Report
Resource Website
RRID:CVCL_5M96 Homo sapiens (Human) Duchenne muscular dystrophy Population: Caucasian., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:21354051
PMID:23665875
Finite cell line Male CLO:CLO_0018945,
Coriell:GM04619,
Wikidata:Q54838604
CVCL_5M96 2026-09-05 10:55:04 0
GM05011
 
Resource Report
Resource Website
Coriell Cat# GM05011, RRID:CVCL_X135 Homo sapiens (Human) Population: Caucasian. PMID:6661932
PMID:23665875
Transformed cell line Female GM-5011, GM 5011, GM05011A Coriell GM05011 CLO:CLO_0025669,
Coriell:GM05011,
Wikidata:Q54838810
CVCL_X135 2026-09-05 10:55:09 0
GM04981
 
Resource Report
Resource Website
RRID:CVCL_8521 Homo sapiens (Human) Becker's muscular dystrophy Population: Caucasian., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:18691744
PMID:21354051
PMID:23665875
Finite cell line Male CLO:CLO_0025653,
Coriell:GM04981,
Wikidata:Q54838791
CVCL_8521 2026-09-05 10:55:09 0
GM05016
 
Resource Report
Resource Website
RRID:CVCL_5N01 Homo sapiens (Human) Duchenne muscular dystrophy PMID:23665875 Transformed cell line Male CLO:CLO_0025677,
Coriell:GM05016,
Wikidata:Q54838812
CVCL_5N01 2026-09-05 10:55:09 0
GM05067
 
Resource Report
Resource Website
RRID:CVCL_M939 Homo sapiens (Human) Trisomy 9 Population: Caribbean; Trinidadian. PMID:6661932
PMID:23665875
Transformed cell line Male GM 5067, GM05067A CLO:CLO_0025332,
Coriell:GM05067,
Wikidata:Q54838841
CVCL_M939 2026-09-05 10:55:10 0
GM05017
 
Resource Report
Resource Website
RRID:CVCL_5N02 Homo sapiens (Human) Duchenne muscular dystrophy PMID:23665875 Finite cell line Male CLO:CLO_0025627,
Coriell:GM05017,
Wikidata:Q54838816
CVCL_5N02 2026-09-05 10:55:09 0
GM04993
 
Resource Report
Resource Website
RRID:CVCL_X314 Homo sapiens (Human) Population: Caucasian. PMID:6661932
PMID:23665875
Finite cell line Female GM 4993 CLO:CLO_0025652,
Coriell:GM04993,
Wikidata:Q54838797
CVCL_X314 2026-09-05 10:55:09 0
GM05112
 
Resource Report
Resource Website
RRID:CVCL_5N08 Homo sapiens (Human) Duchenne muscular dystrophy Population: Caucasian. PMID:23665875 Finite cell line Male CLO:CLO_0025379,
Coriell:GM05112,
Wikidata:Q54838862
CVCL_5N08 2026-09-05 10:55:10 0
GM05082
 
Resource Report
Resource Website
RRID:CVCL_U481 Homo sapiens (Human) Becker's muscular dystrophy Population: Caucasian., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:21354051
PMID:23665875
Transformed cell line Male CLO:CLO_0025338,
Coriell:GM05082,
Wikidata:Q54838845
CVCL_U481 2026-09-05 10:55:10 0

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