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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
GM11958
 
Resource Report
Resource Website
Coriell Cat# GM11958, RRID:CVCL_5L14 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male Coriell GM11958 CLO:CLO_0020108,
Coriell:GM11958,
Wikidata:Q54845390
CVCL_5L14 2026-09-12 05:34:23 0
GM11962
 
Resource Report
Resource Website
Coriell Cat# GM11962, RRID:CVCL_2U17 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM11962 CLO:CLO_0020110,
Coriell:GM11962,
Wikidata:Q54845394
CVCL_2U17 2026-09-12 05:34:23 0
GM11961
 
Resource Report
Resource Website
RRID:CVCL_2U16 Homo sapiens (Human) PMID:23665875 Transformed cell line Female CLO:CLO_0020111,
Coriell:GM11961,
Wikidata:Q54845393
CVCL_2U16 2026-09-12 05:34:23 0
GM11970
 
Resource Report
Resource Website
Coriell Cat# GM11970, RRID:CVCL_N192 Homo sapiens (Human) Potocki-Shaffer syndrome Population: Mexican., Part of: Human variation panel. PMID:23665875 Transformed cell line Female GM17070 Coriell GM11970 CLO:CLO_0014600,
CLO:CLO_0020549,
Coriell:GM11970,
Coriell:GM17070,
Wikidata:Q54845403
CVCL_N192 2026-09-12 05:34:23 0
GM11950
 
Resource Report
Resource Website
RRID:CVCL_5L07 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0020205,
Coriell:GM11950,
Wikidata:Q54845382
CVCL_5L07 2026-09-12 05:34:22 0
GM11948
 
Resource Report
Resource Website
Coriell Cat# GM11948, RRID:CVCL_5L06 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male Coriell GM11948 CLO:CLO_0020215,
Coriell:GM11948,
Wikidata:Q54845380
CVCL_5L06 2026-09-12 05:34:22 0
GM11959
 
Resource Report
Resource Website
Coriell Cat# GM11959, RRID:CVCL_5L15 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male Coriell GM11959 CLO:CLO_0020107,
Coriell:GM11959,
Wikidata:Q54845391
CVCL_5L15 2026-09-12 05:34:23 0
GM11952
 
Resource Report
Resource Website
Coriell Cat# GM11952, RRID:CVCL_5L09 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Female Coriell GM11952 CLO:CLO_0020125,
Coriell:GM11952,
Wikidata:Q54845385
CVCL_5L09 2026-09-12 05:34:22 0
GM11967
 
Resource Report
Resource Website
RRID:CVCL_5L19 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0020540,
Coriell:GM11967,
Wikidata:Q54845400
CVCL_5L19 2026-09-12 05:34:23 0
GM11961
 
Resource Report
Resource Website
Coriell Cat# GM11961, RRID:CVCL_2U16 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM11961 CLO:CLO_0020111,
Coriell:GM11961,
Wikidata:Q54845393
CVCL_2U16 2026-09-12 05:34:23 0
GM11967
 
Resource Report
Resource Website
Coriell Cat# GM11967, RRID:CVCL_5L19 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Female Coriell GM11967 CLO:CLO_0020540,
Coriell:GM11967,
Wikidata:Q54845400
CVCL_5L19 2026-09-12 05:34:23 0
GM11965
 
Resource Report
Resource Website
RRID:CVCL_5L18 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male CLO:CLO_0020544,
Coriell:GM11965,
Wikidata:Q54845398
CVCL_5L18 2026-09-12 05:34:23 0
GM12134
 
Resource Report
Resource Website
Coriell Cat# GM12134, RRID:CVCL_U535 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Male Coriell GM12134 CLO:CLO_0019099,
BioSample:SAMN00801199,
Coriell:GM12134,
Wikidata:Q54845551
CVCL_U535 2026-09-12 05:34:27 0
GM12218
 
Resource Report
Resource Website
RRID:CVCL_5P64 Homo sapiens (Human) PMID:23665875 Finite cell line Female Coriell:GM12218,
Wikidata:Q54845596
CVCL_5P64 2026-09-12 05:34:28 0
GM12519
 
Resource Report
Resource Website
RRID:CVCL_H549 Homo sapiens (Human) PMID:23665875 Finite cell line Female CLO:CLO_0017851,
Coriell:GM12519,
Wikidata:Q54845824
CVCL_H549 2026-09-12 05:34:33 0
GM12606
 
Resource Report
Resource Website
RRID:CVCL_5P66 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0018088,
Coriell:GM12606,
Wikidata:Q54845895
CVCL_5P66 2026-09-12 05:34:35 0
GM12590
 
Resource Report
Resource Website
Coriell Cat# GM12590, RRID:CVCL_5P65 Homo sapiens (Human) PMID:23665875 Finite cell line Male Coriell GM12590 Coriell:GM12590,
Wikidata:Q54845883
CVCL_5P65 2026-09-12 05:34:35 0
GM12722
 
Resource Report
Resource Website
Coriell Cat# GM12722, RRID:CVCL_5P69 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM12722 CLO:CLO_0022568,
Coriell:GM12722,
Wikidata:Q54846003
CVCL_5P69 2026-09-12 05:34:38 0
GM12959
 
Resource Report
Resource Website
RRID:CVCL_5P71 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0022918,
Coriell:GM12959,
Wikidata:Q54846240
CVCL_5P71 2026-09-12 05:34:43 0
GM13164
 
Resource Report
Resource Website
Coriell Cat# GM13164, RRID:CVCL_4W21 Homo sapiens (Human) Rubinstein-Taybi syndrome Population: African American. PMID:23665875 Transformed cell line Female Coriell GM13164 CLO:CLO_0013645,
BioSample:SAMN00802155,
Coriell:GM13164,
Wikidata:Q54846354
CVCL_4W21 2026-09-12 05:34:46 0

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