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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
GM50194
 
Resource Report
Resource Website
Coriell Cat# GM50194, RRID:CVCL_0G72 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Male JL453 Coriell GM50194 CLO:CLO_0014993,
Coriell:GM50194,
Wikidata:Q54854257
CVCL_0G72 2026-09-19 05:33:12 0
GM50205
 
Resource Report
Resource Website
Coriell Cat# GM50205, RRID:CVCL_5T58 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Female Coriell GM50205 BioSample:SAMN00806847,
Coriell:GM50205,
Wikidata:Q54854259
CVCL_5T58 2026-09-19 05:33:12 0
GM50276
 
Resource Report
Resource Website
RRID:CVCL_5T62 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM50276,
Wikidata:Q54854263
CVCL_5T62 2026-09-19 05:33:12 0
GM50186
 
Resource Report
Resource Website
RRID:CVCL_0H55 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Female JL430 CLO:CLO_0014983,
Coriell:GM50186,
Wikidata:Q54854252
CVCL_0H55 2026-09-19 05:33:11 0
GM50215
 
Resource Report
Resource Website
RRID:CVCL_5T59 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Female BioSample:SAMN00806849,
Coriell:GM50215,
Wikidata:Q54854260
CVCL_5T59 2026-09-19 05:33:12 0
GM50188
 
Resource Report
Resource Website
Coriell Cat# GM50188, RRID:CVCL_5T56 Homo sapiens (Human) Cri du chat syndrome Population: Lebanese. PMID:23665875 Transformed cell line Female Coriell GM50188 Coriell:GM50188,
Wikidata:Q54854253
CVCL_5T56 2026-09-19 05:33:11 0
GM50275
 
Resource Report
Resource Website
RRID:CVCL_5T61 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM50275,
Wikidata:Q54854262
CVCL_5T61 2026-09-19 05:33:12 0
GM50178
 
Resource Report
Resource Website
Coriell Cat# GM50178, RRID:CVCL_0G67 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Female JL378 Coriell GM50178 CLO:CLO_0014986,
Coriell:GM50178,
Wikidata:Q54854249
CVCL_0G67 2026-09-19 05:33:11 0
GM50322
 
Resource Report
Resource Website
RRID:CVCL_1U17 Homo sapiens (Human) Deletion 18p syndrome PMID:1577474
PMID:23665875
Transformed cell line Female JL91 CLO:CLO_0012521,
Coriell:GM50322,
Wikidata:Q54854268
CVCL_1U17 2026-09-19 05:33:12 0
GM50323
 
Resource Report
Resource Website
Coriell Cat# GM50323, RRID:CVCL_1U18 Homo sapiens (Human) PMID:23665875 Transformed cell line Female JL92 Coriell GM50323 CLO:CLO_0012520,
Coriell:GM50323,
Wikidata:Q54854269
CVCL_1U18 2026-09-19 05:33:12 0
GM22936
 
Resource Report
Resource Website
RRID:CVCL_5S36 Homo sapiens (Human) 1p36 deletion syndrome PMID:23665875 Transformed cell line Male Coriell:GM22936,
Wikidata:Q54852838
CVCL_5S36 2026-09-19 05:32:22 0
GM22979
 
Resource Report
Resource Website
RRID:CVCL_5S47 Homo sapiens (Human) 1p36 deletion syndrome PMID:23665875 Transformed cell line Female Coriell:GM22979,
Wikidata:Q54852855
CVCL_5S47 2026-09-19 05:32:22 0
GM22908
 
Resource Report
Resource Website
RRID:CVCL_5S24 Homo sapiens (Human) 1p36 deletion syndrome PMID:23665875 Transformed cell line Male Coriell:GM22908,
Wikidata:Q54852822
CVCL_5S24 2026-09-19 05:32:21 0
GM23054
 
Resource Report
Resource Website
RRID:CVCL_5S66 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell:GM23054,
Wikidata:Q54852875
CVCL_5S66 2026-09-19 05:32:23 0
GM22991
 
Resource Report
Resource Website
Coriell Cat# GM22991, RRID:CVCL_5S48 Homo sapiens (Human) 1p36 deletion syndrome PMID:23665875 Transformed cell line Female Coriell GM22991 Coriell:GM22991,
Wikidata:Q54852856
CVCL_5S48 2026-09-19 05:32:22 0
GM22931
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM22931, RRID:CVCL_5S34 Homo sapiens (Human) 1p36 deletion syndrome PMID:23665875 Transformed cell line Male Coriell GM22931 Coriell:GM22931,
Wikidata:Q54852836
CVCL_5S34 2026-09-19 05:32:22 0
GM23002
 
Resource Report
Resource Website
Coriell Cat# GM23002, RRID:CVCL_5S56 Homo sapiens (Human) 1p36 deletion syndrome PMID:23665875 Transformed cell line Female Coriell GM23002 Coriell:GM23002,
Wikidata:Q54852864
CVCL_5S56 2026-09-19 05:32:22 0
GM22927
 
Resource Report
Resource Website
Coriell Cat# GM22927, RRID:CVCL_5S31 Homo sapiens (Human) 1p36 deletion syndrome PMID:23665875 Transformed cell line Female Coriell GM22927 Coriell:GM22927,
Wikidata:Q54852832
CVCL_5S31 2026-09-19 05:32:21 0
GM23053
 
Resource Report
Resource Website
Coriell Cat# GM23053, RRID:CVCL_5S65 Homo sapiens (Human) Charcot-Marie-Tooth disease type 1A PMID:23665875 Transformed cell line Female Coriell GM23053 Coriell:GM23053,
Wikidata:Q54852874
CVCL_5S65 2026-09-19 05:32:23 0
GM22992
 
Resource Report
Resource Website
Coriell Cat# GM22992, RRID:CVCL_5S49 Homo sapiens (Human) 1p36 deletion syndrome PMID:23665875 Transformed cell line Female Coriell GM22992 Coriell:GM22992,
Wikidata:Q54852857
CVCL_5S49 2026-09-19 05:32:22 0

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