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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
GM18311
 
Resource Report
Resource Website
Coriell Cat# GM18311, RRID:CVCL_5Q86 Homo sapiens (Human) Holoprosencephaly PMID:23665875 Transformed cell line Female Coriell GM18311 CLO:CLO_0031073,
Coriell:GM18311,
Wikidata:Q54849489
CVCL_5Q86 2026-09-12 05:35:52 0
GM18332
 
Resource Report
Resource Website
RRID:CVCL_5Q88 Homo sapiens (Human) Azoospermia PMID:23665875 Transformed cell line Male CLO:CLO_0031062,
Coriell:GM18332,
Wikidata:Q54849500
CVCL_5Q88 2026-09-12 05:35:52 0
GM18319
 
Resource Report
Resource Website
Coriell Cat# GM18319, RRID:CVCL_5K12 Homo sapiens (Human) Smith-Magenis syndrome PMID:23665875 Transformed cell line Female Coriell GM18319 CLO:CLO_0031078,
Coriell:GM18319,
Wikidata:Q54849491
CVCL_5K12 2026-09-12 05:35:52 0
GM18340
 
Resource Report
Resource Website
Coriell Cat# GM18340, RRID:CVCL_5Q96 Homo sapiens (Human) Azoospermia PMID:23665875 Transformed cell line Male Coriell GM18340 CLO:CLO_0031114,
Coriell:GM18340,
Wikidata:Q54849508
CVCL_5Q96 2026-09-12 05:35:52 0
GM18335
 
Resource Report
Resource Website
RRID:CVCL_5Q91 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0031069,
Coriell:GM18335,
Wikidata:Q54849503
CVCL_5Q91 2026-09-12 05:35:52 0
GM18319
 
Resource Report
Resource Website
RRID:CVCL_5K12 Homo sapiens (Human) Smith-Magenis syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0031078,
Coriell:GM18319,
Wikidata:Q54849491
CVCL_5K12 2026-09-12 05:35:52 0
GM18331
 
Resource Report
Resource Website
Coriell Cat# GM18331, RRID:CVCL_5Q87 Homo sapiens (Human) Azoospermia PMID:23665875 Transformed cell line Male Coriell GM18331 CLO:CLO_0031063,
Coriell:GM18331,
Wikidata:Q54849499
CVCL_5Q87 2026-09-12 05:35:52 0
GM18323
 
Resource Report
Resource Website
Coriell Cat# GM18323, RRID:CVCL_5K16 Homo sapiens (Human) Smith-Magenis syndrome PMID:23665875 Transformed cell line Female Coriell GM18323 CLO:CLO_0031075,
Coriell:GM18323,
Wikidata:Q54849495
CVCL_5K16 2026-09-12 05:35:52 0
GM18331
 
Resource Report
Resource Website
RRID:CVCL_5Q87 Homo sapiens (Human) Azoospermia PMID:23665875 Transformed cell line Male CLO:CLO_0031063,
Coriell:GM18331,
Wikidata:Q54849499
CVCL_5Q87 2026-09-12 05:35:52 0
GM18324
 
Resource Report
Resource Website
RRID:CVCL_5K17 Homo sapiens (Human) Smith-Magenis syndrome PMID:23665875 Transformed cell line Male CLO:CLO_0031074,
Coriell:GM18324,
Wikidata:Q54849496
CVCL_5K17 2026-09-12 05:35:52 0
GM18326
 
Resource Report
Resource Website
Coriell Cat# GM18326, RRID:CVCL_5K19 Homo sapiens (Human) Smith-Magenis syndrome PMID:23665875 Transformed cell line Male Coriell GM18326 CLO:CLO_0031064,
Coriell:GM18326,
Wikidata:Q54849498
CVCL_5K19 2026-09-12 05:35:52 0
GM18311
 
Resource Report
Resource Website
RRID:CVCL_5Q86 Homo sapiens (Human) Holoprosencephaly PMID:23665875 Transformed cell line Female CLO:CLO_0031073,
Coriell:GM18311,
Wikidata:Q54849489
CVCL_5Q86 2026-09-12 05:35:52 0
GM18332
 
Resource Report
Resource Website
Coriell Cat# GM18332, RRID:CVCL_5Q88 Homo sapiens (Human) Azoospermia PMID:23665875 Transformed cell line Male Coriell GM18332 CLO:CLO_0031062,
Coriell:GM18332,
Wikidata:Q54849500
CVCL_5Q88 2026-09-12 05:35:52 0
GM18337
 
Resource Report
Resource Website
RRID:CVCL_5Q93 Homo sapiens (Human) Azoospermia PMID:23665875 Transformed cell line Male CLO:CLO_0031067,
Coriell:GM18337,
Wikidata:Q54849505
CVCL_5Q93 2026-09-12 05:35:52 0
GM18378
 
Resource Report
Resource Website
RRID:CVCL_5Q97 Homo sapiens (Human) Holoprosencephaly PMID:23665875 Transformed cell line Female Coriell:GM18378,
Wikidata:Q54849517
CVCL_5Q97 2026-09-12 05:35:53 0
GM18381
 
Resource Report
Resource Website
Coriell Cat# GM18381, RRID:CVCL_5Q99 Homo sapiens (Human) Pseudotrisomy 13 syndrome PMID:23665875 Transformed cell line Male Coriell GM18381 CLO:CLO_0031096,
Coriell:GM18381,
Wikidata:Q54849519
CVCL_5Q99 2026-09-12 05:35:53 0
GM18826
 
Resource Report
Resource Website
Coriell Cat# GM18826, RRID:CVCL_2U52 Homo sapiens (Human) Developmental delay Population: Caucasian. PMID:23665875 Transformed cell line Female Coriell GM18826 CLO:CLO_0026218,
Coriell:GM18826,
Wikidata:Q54849860
CVCL_2U52 2026-09-12 05:36:00 0
GM18828
 
Resource Report
Resource Website
RRID:CVCL_2U54 Homo sapiens (Human) Developmental delay Population: Caucasian. PMID:23665875 Transformed cell line Male CLO:CLO_0026216,
Coriell:GM18828,
Wikidata:Q54849862
CVCL_2U54 2026-09-12 05:36:00 0
GM18825
 
Resource Report
Resource Website
Coriell Cat# GM18825, RRID:CVCL_2U51 Homo sapiens (Human) Developmental delay Population: Caucasian. PMID:23665875 Transformed cell line Female Coriell GM18825 CLO:CLO_0026217,
Coriell:GM18825,
Wikidata:Q54849859
CVCL_2U51 2026-09-12 05:36:00 0
GM18827
 
Resource Report
Resource Website
RRID:CVCL_2U53 Homo sapiens (Human) Developmental delay Population: Caucasian. PMID:23665875 Transformed cell line Female CLO:CLO_0026215,
Coriell:GM18827,
Wikidata:Q54849861
CVCL_2U53 2026-09-12 05:36:00 0

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