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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 Authority Record Last Update Mentions Count
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 Cellosaurus 2026-10-31 05:08:38 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 Cellosaurus 2026-10-31 05:08:37 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 Cellosaurus 2026-10-31 05:08:37 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 Cellosaurus 2026-10-31 05:08:37 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 Cellosaurus 2026-10-31 05:08:37 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 Cellosaurus 2026-10-31 05:08:37 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 Cellosaurus 2026-10-31 05:08:38 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 Cellosaurus 2026-10-31 05:08:37 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 Cellosaurus 2026-10-31 05:08:37 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 Cellosaurus 2026-10-31 05:08:37 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 Cellosaurus 2026-10-31 05:08:37 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 Cellosaurus 2026-10-31 05:08:37 0
GM23697
 
Resource Report
Resource Website
RRID:CVCL_5T03 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell:GM23697,
Wikidata:Q54853242
CVCL_5T03 Cellosaurus 2026-10-31 05:08:00 0
GM23702
 
Resource Report
Resource Website
Coriell Cat# GM23702, RRID:CVCL_5T08 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM23702 Coriell:GM23702,
Wikidata:Q54853247
CVCL_5T08 Cellosaurus 2026-10-31 05:08:00 0
GM23675
 
Resource Report
Resource Website
RRID:CVCL_5S97 Homo sapiens (Human) Lubs X-linked intellectual disability syndrome Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:23665875
PMID:24508304
Transformed cell line Male Coriell:GM23675,
Wikidata:Q54853218
CVCL_5S97 Cellosaurus 2026-10-31 05:07:59 0
GM23708
 
Resource Report
Resource Website
Coriell Cat# GM23708, RRID:CVCL_5T11 Homo sapiens (Human) Chromosome 15q11-q13 duplication syndrome PMID:23665875 Transformed cell line Female Coriell GM23708 Coriell:GM23708,
Wikidata:Q54853253
CVCL_5T11 Cellosaurus 2026-10-31 05:08:00 0
GM23698
 
Resource Report
Resource Website
Coriell Cat# GM23698, RRID:CVCL_5T04 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM23698 Coriell:GM23698,
Wikidata:Q54853243
CVCL_5T04 Cellosaurus 2026-10-31 05:08:00 0
GM23708
 
Resource Report
Resource Website
RRID:CVCL_5T11 Homo sapiens (Human) Chromosome 15q11-q13 duplication syndrome PMID:23665875 Transformed cell line Female Coriell:GM23708,
Wikidata:Q54853253
CVCL_5T11 Cellosaurus 2026-10-31 05:08:00 0
GM23696
 
Resource Report
Resource Website
RRID:CVCL_5T02 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM23696,
Wikidata:Q54853241
CVCL_5T02 Cellosaurus 2026-10-31 05:08:00 0
GM23713
 
Resource Report
Resource Website
Coriell Cat# GM23713, RRID:CVCL_5T14 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM23713 Coriell:GM23713,
Wikidata:Q54853258
CVCL_5T14 Cellosaurus 2026-10-31 05:08:00 0

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