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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
GM16598
 
Resource Report
Resource Website
RRID:CVCL_5Q74 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Male JL88 CLO:CLO_0017405,
Coriell:GM16598,
Wikidata:Q54848671
CVCL_5Q74 2026-09-12 05:35:37 0
GM16586
 
Resource Report
Resource Website
Coriell Cat# GM16586, RRID:CVCL_0G75 Homo sapiens (Human) Holoprosencephaly PMID:7485158
PMID:23665875
Transformed cell line Male JL218 Coriell GM16586 CLO:CLO_0017390,
Coriell:GM16586,
Wikidata:Q54848646
CVCL_0G75 2026-09-12 05:35:37 0
GM16718
 
Resource Report
Resource Website
RRID:CVCL_5Q76 Homo sapiens (Human) Azoospermia Population: Southeast Asian; Vietnamese. PMID:23665875 Transformed cell line Male CLO:CLO_0018424,
Coriell:GM16718,
Wikidata:Q54848711
CVCL_5Q76 2026-09-12 05:35:38 0
GM16580
 
Resource Report
Resource Website
RRID:CVCL_5Q68 Homo sapiens (Human) Deletion 18p syndrome PMID:23665875 Transformed cell line Male JL462 Coriell:GM16580,
Wikidata:Q54848641
CVCL_5Q68 2026-09-12 05:35:37 0
GM16598
 
Resource Report
Resource Website
Coriell Cat# GM16598, RRID:CVCL_5Q74 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Male JL88 Coriell GM16598 CLO:CLO_0017405,
Coriell:GM16598,
Wikidata:Q54848671
CVCL_5Q74 2026-09-12 05:35:37 0
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 2026-09-12 05:35:37 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 2026-09-12 05:35:37 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 2026-09-12 05:35:38 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 2026-09-12 05:35:37 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 2026-09-12 05:35:37 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 2026-09-12 05:35:39 0
GM16809
 
Resource Report
Resource Website
RRID:CVCL_5Q80 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM16809,
Wikidata:Q54848756
CVCL_5Q80 2026-09-12 05:35:39 0
GM16808
 
Resource Report
Resource Website
RRID:CVCL_5Q79 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell:GM16808,
Wikidata:Q54848755
CVCL_5Q79 2026-09-12 05:35:39 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 2026-09-12 05:35:39 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 2026-09-12 05:35:40 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 2026-09-12 05:35:40 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 2026-09-12 05:35:39 0
GM14523
 
Resource Report
Resource Website
Coriell Cat# GM14523, RRID:CVCL_2U42 Homo sapiens (Human) PMID:23665875 Finite cell line Female Coriell GM14523 CLO:CLO_0031598,
Coriell:GM14523,
Wikidata:Q54847273
CVCL_2U42 2026-09-12 05:35:07 0
GM14946
 
Resource Report
Resource Website
Coriell Cat# GM14946, RRID:CVCL_H545 Homo sapiens (Human) PMID:23665875 Finite cell line Male Coriell GM14946 CLO:CLO_0030459,
Coriell:GM14946,
Wikidata:Q54847538
CVCL_H545 2026-09-12 05:35:13 0
GM15012
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_5V23 Homo sapiens (Human) Angelman syndrome PMID:23665875 Transformed cell line Male Coriell:GM15012,
Wikidata:Q54847566
CVCL_5V23 2026-09-12 05:35:13 0

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