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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
GM50142
 
Resource Report
Resource Website
Coriell Cat# GM50142, RRID:CVCL_5T49 Homo sapiens (Human) PMID:23665875 Transformed cell line Male JL263 Coriell GM50142 CLO:CLO_0014676,
Coriell:GM50142,
Wikidata:Q54854217
CVCL_5T49 2026-02-14 08:21:11 0
GM50125
 
Resource Report
Resource Website
RRID:CVCL_0F94 Homo sapiens (Human) Deletion 18q syndrome PMID:8488839
PMID:23665875
Transformed cell line Female JL209 CLO:CLO_0014669,
Coriell:GM50125,
Wikidata:Q54854210
CVCL_0F94 2026-02-14 08:21:11 0
GM50324
 
Resource Report
Resource Website
RRID:CVCL_5T64 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM50324,
Wikidata:Q54854270
CVCL_5T64 2026-02-14 08:21:13 0
GM50248
 
Resource Report
Resource Website
RRID:CVCL_5T60 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Male Coriell:GM50248,
Wikidata:Q54854261
CVCL_5T60 2026-02-14 08:21:13 0
GM50284
 
Resource Report
Resource Website
Coriell Cat# GM50284, RRID:CVCL_5T63 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Female Coriell GM50284 Coriell:GM50284,
Wikidata:Q54854264
CVCL_5T63 2026-02-14 08:21:13 0
GM50193
 
Resource Report
Resource Website
RRID:CVCL_5L36 Homo sapiens (Human) Deletion 18p syndrome PMID:23665875 Transformed cell line Female JL451 CLO:CLO_0014989,
Coriell:GM50193,
Wikidata:Q54854256
CVCL_5L36 2026-02-14 08:21:13 0
GM50322
 
Resource Report
Resource Website
Coriell Cat# GM50322, RRID:CVCL_1U17 Homo sapiens (Human) Deletion 18p syndrome PMID:1577474
PMID:23665875
Transformed cell line Female JL91 Coriell GM50322 CLO:CLO_0012521,
Coriell:GM50322,
Wikidata:Q54854268
CVCL_1U17 2026-02-14 08:21:13 0
GM50284
 
Resource Report
Resource Website
RRID:CVCL_5T63 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Female Coriell:GM50284,
Wikidata:Q54854264
CVCL_5T63 2026-02-14 08:21:13 0
GM50186
 
Resource Report
Resource Website
Coriell Cat# GM50186, RRID:CVCL_0H55 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Female JL430 Coriell GM50186 CLO:CLO_0014983,
Coriell:GM50186,
Wikidata:Q54854252
CVCL_0H55 2026-02-14 08:21:12 0
GM50182
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM50182, RRID:CVCL_5T55 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM50182 Coriell:GM50182,
Wikidata:Q54854251
CVCL_5T55 2026-02-14 08:21:12 0
GM50188
 
Resource Report
Resource Website
RRID:CVCL_5T56 Homo sapiens (Human) Cri du chat syndrome Population: Lebanese. PMID:23665875 Transformed cell line Female Coriell:GM50188,
Wikidata:Q54854253
CVCL_5T56 2026-02-14 08:21:12 0
GM50180
 
Resource Report
Resource Website
RRID:CVCL_5L35 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male JL393 CLO:CLO_0014980,
Coriell:GM50180,
Wikidata:Q54854250
CVCL_5L35 2026-02-14 08:21:12 0
GM50248
 
Resource Report
Resource Website
Coriell Cat# GM50248, RRID:CVCL_5T60 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Male Coriell GM50248 Coriell:GM50248,
Wikidata:Q54854261
CVCL_5T60 2026-02-14 08:21:13 0
GM50276
 
Resource Report
Resource Website
Coriell Cat# GM50276, RRID:CVCL_5T62 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM50276 Coriell:GM50276,
Wikidata:Q54854263
CVCL_5T62 2026-02-14 08:21:13 0
GM50180
 
Resource Report
Resource Website
Coriell Cat# GM50180, RRID:CVCL_5L35 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male JL393 Coriell GM50180 CLO:CLO_0014980,
Coriell:GM50180,
Wikidata:Q54854250
CVCL_5L35 2026-02-14 08:21:12 0
GM50215
 
Resource Report
Resource Website
Coriell Cat# GM50215, RRID:CVCL_5T59 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Female Coriell GM50215 BioSample:SAMN00806849,
Coriell:GM50215,
Wikidata:Q54854260
CVCL_5T59 2026-02-14 08:21:13 0
GM50182
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_5T55 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell:GM50182,
Wikidata:Q54854251
CVCL_5T55 2026-02-14 08:21:12 0
GM50194
 
Resource Report
Resource Website
RRID:CVCL_0G72 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Male JL453 CLO:CLO_0014993,
Coriell:GM50194,
Wikidata:Q54854257
CVCL_0G72 2026-02-14 08:21:13 0
GM50205
 
Resource Report
Resource Website
RRID:CVCL_5T58 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Female BioSample:SAMN00806847,
Coriell:GM50205,
Wikidata:Q54854259
CVCL_5T58 2026-02-14 08:21:13 0
GM23504
 
Resource Report
Resource Website
Coriell Cat# GM23504, RRID:CVCL_5S95 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM23504 Coriell:GM23504,
Wikidata:Q54853125
CVCL_5S95 2026-02-14 08:20:27 0

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