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  • References:pmid:23665875 (facet)

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1,669 Results - per page

Show More Columns | Download Top 1000 Results

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
GM16593
 
Resource Report
Resource Website
RRID:CVCL_5Q71 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Female JL444 CLO:CLO_0017398,
Coriell:GM16593,
Wikidata:Q54848668
CVCL_5Q71 2026-09-05 10:58:03 0
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 2026-09-05 10:58:03 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 2026-09-05 10:58:04 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 2026-09-05 10:58:03 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 2026-09-05 10:58:03 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 2026-09-05 10:58:05 0
GM16809
 
Resource Report
Resource Website
RRID:CVCL_5Q80 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM16809,
Wikidata:Q54848756
CVCL_5Q80 2026-09-05 10:58:05 0
GM16808
 
Resource Report
Resource Website
RRID:CVCL_5Q79 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell:GM16808,
Wikidata:Q54848755
CVCL_5Q79 2026-09-05 10:58:05 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 2026-09-05 10:58:05 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 2026-09-05 10:58:06 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 2026-09-05 10:58:06 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 2026-09-05 10:58:06 0
GM19926
 
Resource Report
Resource Website
Coriell Cat# GM19926, RRID:CVCL_F098 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM19926 CLO:CLO_0028382,
Coriell:GM19926,
Wikidata:Q54850758
CVCL_F098 2026-09-05 10:58:46 0
GM20125
 
Resource Report
Resource Website
RRID:CVCL_5R03 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0027716,
Coriell:GM20125,
Wikidata:Q54850808
CVCL_5R03 2026-09-05 10:58:47 0
GM20027
 
Resource Report
Resource Website
RRID:CVCL_2N06 Homo sapiens (Human) Turner syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0028353,
Coriell:GM20027,
Wikidata:Q54850785
CVCL_2N06 2026-09-05 10:58:46 0
GM19999
 
Resource Report
Resource Website
RRID:CVCL_F105 Homo sapiens (Human) PMID:23665875 Transformed cell line Female CLO:CLO_0028367,
Coriell:GM19999,
Wikidata:Q54850769
CVCL_F105 2026-09-05 10:58:46 0
GM20201
 
Resource Report
Resource Website
Coriell Cat# GM20201, RRID:CVCL_5R05 Homo sapiens (Human) Autism spectrum disorder PMID:23665875 Transformed cell line Female Coriell GM20201 CLO:CLO_0027994,
Coriell:GM20201,
Wikidata:Q54850842
CVCL_5R05 2026-09-05 10:58:47 0
GM20087
 
Resource Report
Resource Website
Coriell Cat# GM20087, RRID:CVCL_5T66 Homo sapiens (Human) Lennox-Gastaut syndrome Population: African American. PMID:23665875 Transformed cell line Female Coriell GM20087 CLO:CLO_0028310,
Coriell:GM20087,
Wikidata:Q54850794
CVCL_5T66 2026-09-05 10:58:46 0
GM20087
 
Resource Report
Resource Website
RRID:CVCL_5T66 Homo sapiens (Human) Lennox-Gastaut syndrome Population: African American. PMID:23665875 Transformed cell line Female CLO:CLO_0028310,
Coriell:GM20087,
Wikidata:Q54850794
CVCL_5T66 2026-09-05 10:58:46 0
GM20022
 
Resource Report
Resource Website
RRID:CVCL_5R01 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0028340,
Coriell:GM20022,
Wikidata:Q54850784
CVCL_5R01 2026-09-05 10:58:46 0

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