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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
GM11571
 
Resource Report
Resource Website
Coriell Cat# GM11571, RRID:CVCL_5P59 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM11571 CLO:CLO_0021052,
Coriell:GM11571,
Wikidata:Q54845160
CVCL_5P59 2026-09-12 05:34:17 0
GM11570
 
Resource Report
Resource Website
Coriell Cat# GM11570, RRID:CVCL_5P58 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM11570 CLO:CLO_0021051,
Coriell:GM11570,
Wikidata:Q54845159
CVCL_5P58 2026-09-12 05:34:17 0
GM11672
 
Resource Report
Resource Website
RRID:CVCL_5P60 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0021332,
Coriell:GM11672,
Wikidata:Q54845214
CVCL_5P60 2026-09-12 05:34:18 0
GM11957
 
Resource Report
Resource Website
Coriell Cat# GM11957, RRID:CVCL_5L13 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Female Coriell GM11957 CLO:CLO_0020109,
Coriell:GM11957,
Wikidata:Q54845389
CVCL_5L13 2026-09-12 05:34:22 0
GM11949
 
Resource Report
Resource Website
RRID:CVCL_5P61 Homo sapiens (Human) PMID:23665875 Transformed cell line Female CLO:CLO_0020203,
Coriell:GM11949,
Wikidata:Q54845381
CVCL_5P61 2026-09-12 05:34:22 0
GM11962
 
Resource Report
Resource Website
RRID:CVCL_2U17 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0020110,
Coriell:GM11962,
Wikidata:Q54845394
CVCL_2U17 2026-09-12 05:34:23 0
GM11957
 
Resource Report
Resource Website
RRID:CVCL_5L13 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0020109,
Coriell:GM11957,
Wikidata:Q54845389
CVCL_5L13 2026-09-12 05:34:22 0
GM11964
 
Resource Report
Resource Website
RRID:CVCL_5L17 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male CLO:CLO_0020539,
Coriell:GM11964,
Wikidata:Q54845397
CVCL_5L17 2026-09-12 05:34:23 0
GM11954
 
Resource Report
Resource Website
RRID:CVCL_5L11 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0020123,
Coriell:GM11954,
Wikidata:Q54845387
CVCL_5L11 2026-09-12 05:34:22 0
GM11965
 
Resource Report
Resource Website
Coriell Cat# GM11965, RRID:CVCL_5L18 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male Coriell GM11965 CLO:CLO_0020544,
Coriell:GM11965,
Wikidata:Q54845398
CVCL_5L18 2026-09-12 05:34:23 0
GM11951
 
Resource Report
Resource Website
RRID:CVCL_5L08 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0020208,
Coriell:GM11951,
Wikidata:Q54845383
CVCL_5L08 2026-09-12 05:34:22 0
GM11951
 
Resource Report
Resource Website
Coriell Cat# GM11951, RRID:CVCL_5L08 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Female Coriell GM11951 CLO:CLO_0020208,
Coriell:GM11951,
Wikidata:Q54845383
CVCL_5L08 2026-09-12 05:34:22 0
GM11964
 
Resource Report
Resource Website
Coriell Cat# GM11964, RRID:CVCL_5L17 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male Coriell GM11964 CLO:CLO_0020539,
Coriell:GM11964,
Wikidata:Q54845397
CVCL_5L17 2026-09-12 05:34:23 0
GM11953
 
Resource Report
Resource Website
RRID:CVCL_5L10 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0020126,
Coriell:GM11953,
Wikidata:Q54845386
CVCL_5L10 2026-09-12 05:34:22 0
GM11970
 
Resource Report
Resource Website
RRID:CVCL_N192 Homo sapiens (Human) Potocki-Shaffer syndrome Population: Mexican., Part of: Human variation panel. PMID:23665875 Transformed cell line Female GM17070 CLO:CLO_0014600,
CLO:CLO_0020549,
Coriell:GM11970,
Coriell:GM17070,
Wikidata:Q54845403
CVCL_N192 2026-09-12 05:34:23 0
GM11959
 
Resource Report
Resource Website
RRID:CVCL_5L15 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male CLO:CLO_0020107,
Coriell:GM11959,
Wikidata:Q54845391
CVCL_5L15 2026-09-12 05:34:23 0
GM11955
 
Resource Report
Resource Website
Coriell Cat# GM11955, RRID:CVCL_5L12 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Female Coriell GM11955 CLO:CLO_0020124,
Coriell:GM11955,
Wikidata:Q54845388
CVCL_5L12 2026-09-12 05:34:22 0
GM11968
 
Resource Report
Resource Website
Coriell Cat# GM11968, RRID:CVCL_5L20 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM11968 CLO:CLO_0020543,
Coriell:GM11968,
Wikidata:Q54845402
CVCL_5L20 2026-09-12 05:34:23 0
GM11950
 
Resource Report
Resource Website
Coriell Cat# GM11950, RRID:CVCL_5L07 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Female Coriell GM11950 CLO:CLO_0020205,
Coriell:GM11950,
Wikidata:Q54845382
CVCL_5L07 2026-09-12 05:34:22 0
GM11948
 
Resource Report
Resource Website
RRID:CVCL_5L06 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male CLO:CLO_0020215,
Coriell:GM11948,
Wikidata:Q54845380
CVCL_5L06 2026-09-12 05:34:22 0

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