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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
GM08755
 
Resource Report
Resource Website
RRID:CVCL_2T57 Homo sapiens (Human) PMID:23665875 Finite cell line Male CLO:CLO_0010509,
BioSample:SAMN00798162,
Coriell:GM08755,
Wikidata:Q54843262
CVCL_2T57 2026-09-05 10:55:54 0
GM08763
 
Resource Report
Resource Website
RRID:CVCL_5N88 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0010492,
BioSample:SAMN00798170,
Coriell:GM08763,
Wikidata:Q54843270
CVCL_5N88 2026-09-05 10:55:55 0
GM08778
 
Resource Report
Resource Website
RRID:CVCL_5N89 Homo sapiens (Human) PMID:23665875 Finite cell line Male CLO:CLO_0010486,
BioSample:SAMN00798194,
Coriell:GM08778,
Wikidata:Q54843293
CVCL_5N89 2026-09-05 10:55:55 0
GM08773
 
Resource Report
Resource Website
Coriell Cat# GM08773, RRID:CVCL_2T58 Homo sapiens (Human) Population: Caucasian. PMID:23665875 Transformed cell line Female Coriell GM08773 CLO:CLO_0010479,
BioSample:SAMN00798186,
Coriell:GM08773,
Wikidata:Q54843289
CVCL_2T58 2026-09-05 10:55:55 0
GM08785
 
Resource Report
Resource Website
RRID:CVCL_5N90 Homo sapiens (Human) WAGR syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0010483,
BioSample:SAMN00798200,
Coriell:GM08785,
Wikidata:Q54843296
CVCL_5N90 2026-09-05 10:55:55 0
GM08946
 
Resource Report
Resource Website
RRID:CVCL_5N93 Homo sapiens (Human) Population: Caucasian. PMID:23665875 Finite cell line Female CLO:CLO_0011042,
BioSample:SAMN00798296,
Coriell:GM08946,
Wikidata:Q54843421
CVCL_5N93 2026-09-05 10:55:58 0
GM08946
 
Resource Report
Resource Website
Coriell Cat# GM08946, RRID:CVCL_5N93 Homo sapiens (Human) Population: Caucasian. PMID:23665875 Finite cell line Female Coriell GM08946 CLO:CLO_0011042,
BioSample:SAMN00798296,
Coriell:GM08946,
Wikidata:Q54843421
CVCL_5N93 2026-09-05 10:55:58 0
GM04371
 
Resource Report
Resource Website
Coriell Cat# GM04371, RRID:CVCL_X305 Homo sapiens (Human) PMID:6661932
PMID:23665875
Finite cell line Male GM-4371, GM 4371 Coriell GM04371 CLO:CLO_0019302,
Coriell:GM04371,
Wikidata:Q54838502
CVCL_X305 2026-09-05 10:55:02 0
GM04409
 
Resource Report
Resource Website
RRID:CVCL_F124 Homo sapiens (Human) Population: Caucasian. PMID:6661932
PMID:23665875
Finite cell line Male GM-4409, GM 4409 CLO:CLO_0019707,
Coriell:GM04409,
Wikidata:Q54838516
CVCL_F124 2026-09-05 10:55:02 0
GM04300
 
Resource Report
Resource Website
Coriell Cat# GM04300, RRID:CVCL_N016 Homo sapiens (Human) Intellectual developmental disorder Population: Indian., Part of: Human variation panel. PMID:23665875 Finite cell line Female GM17023 Coriell GM04300 CLO:CLO_0014707,
CLO:CLO_0019627,
Coriell:GM04300,
Coriell:GM17023,
Wikidata:Q54838473
CVCL_N016 2026-09-05 10:55:02 0
GM04300
 
Resource Report
Resource Website
RRID:CVCL_N016 Homo sapiens (Human) Intellectual developmental disorder Population: Indian., Part of: Human variation panel. PMID:23665875 Finite cell line Female GM17023 CLO:CLO_0014707,
CLO:CLO_0019627,
Coriell:GM04300,
Coriell:GM17023,
Wikidata:Q54838473
CVCL_N016 2026-09-05 10:55:01 0
GM04371
 
Resource Report
Resource Website
RRID:CVCL_X305 Homo sapiens (Human) PMID:6661932
PMID:23665875
Finite cell line Male GM-4371, GM 4371 CLO:CLO_0019302,
Coriell:GM04371,
Wikidata:Q54838502
CVCL_X305 2026-09-05 10:55:02 0
GM04375
 
Resource Report
Resource Website
RRID:CVCL_W622 Homo sapiens (Human) Klinefelter syndrome Population: Caucasian. PMID:6661932
PMID:23665875
Finite cell line Male GM04375A CLO:CLO_0019338,
Coriell:GM04375,
Wikidata:Q54838507
CVCL_W622 2026-09-05 10:55:02 0
GM04297
 
Resource Report
Resource Website
RRID:CVCL_5M91 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0019633,
Coriell:GM04297,
Wikidata:Q54838472
CVCL_5M91 2026-09-05 10:55:01 0
GM04315
 
Resource Report
Resource Website
RRID:CVCL_5M92 Homo sapiens (Human) Population: African American., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:21354051
PMID:23665875
Finite cell line Female CLO:CLO_0019552,
Coriell:GM04315,
Wikidata:Q54838479
CVCL_5M92 2026-09-05 10:55:02 0
GM04592
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_V473 Homo sapiens (Human) Down syndrome Population: Caucasian. PMID:6661932
PMID:23665875
Finite cell line Female GM 4592, GM04592A CLO:CLO_0018882,
Coriell:GM04592,
Wikidata:Q54838578
CVCL_V473 2026-09-05 10:55:04 1
GM04501
 
Resource Report
Resource Website
RRID:CVCL_7409 Homo sapiens (Human) Donor information: Established from monozygotic twin of GM04502 (Cellosaurus=CVCL_F135). PMID:23665875
PMID:30567591
Finite cell line Male GM04501A, HF20 CLO:CLO_0018819,
Coriell:GM04501,
GEO:GSM3124646,
Wikidata:Q54838541
CVCL_7409 2026-09-05 10:55:03 0
GM04626
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM04626, RRID:CVCL_X310 Homo sapiens (Human) PMID:6661932
PMID:21177337
PMID:23665875
Finite cell line Female GM 4626 Coriell GM04626 CLO:CLO_0018940,
Coriell:GM04626,
GEO:GSM608319,
GEO:GSM608320,
Wikidata:Q54838608
CVCL_X310 2026-09-05 10:55:04 1
GM04626
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_X310 Homo sapiens (Human) PMID:6661932
PMID:21177337
PMID:23665875
Finite cell line Female GM 4626 CLO:CLO_0018940,
Coriell:GM04626,
GEO:GSM608319,
GEO:GSM608320,
Wikidata:Q54838608
CVCL_X310 2026-09-05 10:55:04 1
GM04619
 
Resource Report
Resource Website
RRID:CVCL_5M96 Homo sapiens (Human) Duchenne muscular dystrophy Population: Caucasian., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:21354051
PMID:23665875
Finite cell line Male CLO:CLO_0018945,
Coriell:GM04619,
Wikidata:Q54838604
CVCL_5M96 2026-09-05 10:55:04 0

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