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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
GM16584
 
Resource Report
Resource Website
Coriell Cat# GM16584, RRID:CVCL_0G74 Homo sapiens (Human) Holoprosencephaly PMID:23665875 Transformed cell line Female JL257 Coriell GM16584 CLO:CLO_0017548,
Coriell:GM16584,
Wikidata:Q54848644
CVCL_0G74 2026-02-14 08:18:50 0
GM16718
 
Resource Report
Resource Website
Coriell Cat# GM16718, RRID:CVCL_5Q76 Homo sapiens (Human) Azoospermia Population: Southeast Asian; Vietnamese. PMID:23665875 Transformed cell line Male Coriell GM16718 CLO:CLO_0018424,
Coriell:GM16718,
Wikidata:Q54848711
CVCL_5Q76 2026-02-14 08:18:51 0
GM16580
 
Resource Report
Resource Website
Coriell Cat# GM16580, RRID:CVCL_5Q68 Homo sapiens (Human) Deletion 18p syndrome PMID:23665875 Transformed cell line Male JL462 Coriell GM16580 Coriell:GM16580,
Wikidata:Q54848641
CVCL_5Q68 2026-02-14 08:18:50 0
GM16582
 
Resource Report
Resource Website
RRID:CVCL_0G73 Homo sapiens (Human) Holoprosencephaly PMID:23665875 Transformed cell line Male JL376 CLO:CLO_0017552,
Coriell:GM16582,
Wikidata:Q54848642
CVCL_0G73 2026-02-14 08:18:50 0
GM16809
 
Resource Report
Resource Website
Coriell Cat# GM16809, RRID:CVCL_5Q80 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM16809 Coriell:GM16809,
Wikidata:Q54848756
CVCL_5Q80 2026-02-14 08:18:52 0
GM16809
 
Resource Report
Resource Website
RRID:CVCL_5Q80 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM16809,
Wikidata:Q54848756
CVCL_5Q80 2026-02-14 08:18:52 0
GM16808
 
Resource Report
Resource Website
RRID:CVCL_5Q79 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell:GM16808,
Wikidata:Q54848755
CVCL_5Q79 2026-02-14 08:18:52 0
GM16810
 
Resource Report
Resource Website
Coriell Cat# GM16810, RRID:CVCL_5Q81 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM16810 Coriell:GM16810,
Wikidata:Q54848757
CVCL_5Q81 2026-02-14 08:18:52 0
GM17437
 
Resource Report
Resource Website
RRID:CVCL_4E15 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0012909,
Coriell:GM17437,
Wikidata:Q54848874
CVCL_4E15 2026-02-14 08:18:53 0
GM17437
 
Resource Report
Resource Website
Coriell Cat# GM17437, RRID:CVCL_4E15 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM17437 CLO:CLO_0012909,
Coriell:GM17437,
Wikidata:Q54848874
CVCL_4E15 2026-02-14 08:18:53 0
GM16994
 
Resource Report
Resource Website
Coriell Cat# GM16994, RRID:CVCL_2N34 Homo sapiens (Human) Autism spectrum disorder PMID:23665875 Transformed cell line Male Coriell GM16994 Coriell:GM16994,
Wikidata:Q54848827
CVCL_2N34 2026-02-14 08:18:53 0
GM01941
 
Resource Report
Resource Website
Coriell Cat# GM01941, RRID:CVCL_X084 Homo sapiens (Human) Turner syndrome Population: Caucasian. PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Female GM-1941, GM 1941 Coriell GM01941 CLO:CLO_0032323,
BioSample:SAMN00807328,
Coriell:GM01941,
Wikidata:Q54837198
CVCL_X084 2026-02-14 08:14:52 0
GM02030
 
Resource Report
Resource Website
RRID:CVCL_X259 Homo sapiens (Human) Trisomy 8 Population: Caucasian. PMID:6661932
PMID:23665875
Finite cell line Male GM-2030, GM 2030 CLO:CLO_0032576,
BioSample:SAMN00807404,
Coriell:GM02030,
Wikidata:Q54837249
CVCL_X259 2026-02-14 08:14:53 0
GM02025
 
Resource Report
Resource Website
RRID:CVCL_V825 Homo sapiens (Human) Population: Caucasian. PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Male GM-2025, GM 2025, GM2025 CLO:CLO_0032577,
BioSample:SAMN00807400,
Coriell:GM02025,
Wikidata:Q54837244
CVCL_V825 2026-02-14 08:14:53 0
GM02018
 
Resource Report
Resource Website
Coriell Cat# GM02018, RRID:CVCL_V814 Homo sapiens (Human) Population: Caucasian. PMID:456042
PMID:6661932
PMID:23665875
Finite cell line Female GM-2018, GM 2018 Coriell GM02018 CLO:CLO_0032317,
BioSample:SAMN00807394,
Coriell:GM02018,
Wikidata:Q54837241
CVCL_V814 2026-02-14 08:14:53 0
GM02008
 
Resource Report
Resource Website
Coriell Cat# GM02008, RRID:CVCL_X086 Homo sapiens (Human) Population: African American. PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Female GM-2008, GM 2008 Coriell GM02008 CLO:CLO_0032298,
BioSample:SAMN00807378,
Coriell:GM02008,
Wikidata:Q54837233
CVCL_X086 2026-02-14 08:14:53 0
GM02018
 
Resource Report
Resource Website
RRID:CVCL_V814 Homo sapiens (Human) Population: Caucasian. PMID:456042
PMID:6661932
PMID:23665875
Finite cell line Female GM-2018, GM 2018 CLO:CLO_0032317,
BioSample:SAMN00807394,
Coriell:GM02018,
Wikidata:Q54837241
CVCL_V814 2026-02-14 08:14:53 0
GM02206
 
Resource Report
Resource Website
Discontinued
Coriell Cat# GM01514, RRID:CVCL_L969 Homo sapiens (Human) Ehlers-Danlos syndrome Population: Caucasian. PMID:6617268
PMID:23665875
PMID:25326100
Finite cell line Female GM-2206 GM 2206, GM01514 Coriell GM01514 CLO:CLO_0032262,
BioSample:SAMN00807604,
Coriell:GM01514,
Coriell:GM02206,
GEO:GSM1266977,
Wikidata:Q54837370
CVCL_L969 2026-02-14 08:14:56 0
GM02206
 
Resource Report
Resource Website
Discontinued
Coriell Cat# GM02206, RRID:CVCL_L969 Homo sapiens (Human) Ehlers-Danlos syndrome Population: Caucasian. PMID:6617268
PMID:23665875
PMID:25326100
Finite cell line Female GM-2206 GM 2206, GM01514 Coriell GM02206 CLO:CLO_0032262,
BioSample:SAMN00807604,
Coriell:GM01514,
Coriell:GM02206,
GEO:GSM1266977,
Wikidata:Q54837370
CVCL_L969 2026-02-14 08:14:56 0
GM02205
 
Resource Report
Resource Website
Discontinued
Coriell Cat# GM02205, RRID:CVCL_L968 Homo sapiens (Human) Population: Caucasian. PMID:6617268
PMID:23665875
PMID:24555846
PMID:25326100
Finite cell line Male GM-2205, GM 2205, GM01515 Coriell GM02205 CLO:CLO_0032263,
BioSample:SAMN00807602,
Coriell:GM01515,
Coriell:GM02205,
GEO:GSM1266975,
GEO:GSM1267054,
GEO:GSM1288438,
Wikidata:Q54837369
CVCL_L968 2026-02-14 08:14:56 0

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