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256,031 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
GM04617
 
Resource Report
Resource Website
Coriell Cat# GM04617, RRID:CVCL_V476 Homo sapiens (Human) Down syndrome Karyotypic information: 47,XX,+21[25].arr(21)x3 (Coriell=GM04617)., Population: Puerto Rican. PMID:6661932 Finite cell line Female GM 4617 Coriell GM04617 CLO:CLO_0018953,
Coriell:GM04617,
Wikidata:Q54838602
CVCL_V476 2026-07-25 04:33:00 0
GM04717
 
Resource Report
Resource Website
RRID:CVCL_V568 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Female CLO:CLO_0019021,
Coriell:GM04717,
Wikidata:Q54838649
CVCL_V568 2026-07-25 04:33:01 0
GM04711
 
Resource Report
Resource Website
Coriell Cat# GM04711, RRID:CVCL_1I27 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. PMID:6230415 Finite cell line Male GM 4711 Coriell GM04711 CLO:CLO_0019018,
Coriell:GM04711,
Wikidata:Q54838645
CVCL_1I27 2026-07-25 04:33:01 0
GM04693
 
Resource Report
Resource Website
RRID:CVCL_Y878 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Male CLO:CLO_0019032,
Coriell:GM04693,
Wikidata:Q54838635
CVCL_Y878 2026-07-25 04:33:00 0
GM04648
 
Resource Report
Resource Website
RRID:CVCL_AW56 Homo sapiens (Human) Dystrophia myotonica 1 Population: Caucasian., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:23680132
PMID:32656337
Transformed cell line Male CLO:CLO_0018967,
Coriell:GM04648,
Wikidata:Q54838619
CVCL_AW56 2026-07-25 04:33:00 0
GM04721
 
Resource Report
Resource Website
Coriell Cat# GM04721, RRID:CVCL_Y869 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. PMID:6230415 Finite cell line Female GM 4721 Coriell GM04721 CLO:CLO_0019074,
Coriell:GM04721,
Wikidata:Q54838653
CVCL_Y869 2026-07-25 04:33:01 0
GM04729
 
Resource Report
Resource Website
RRID:CVCL_Y882 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. PMID:6230415 Finite cell line Female GM 4729 CLO:CLO_0019071,
Coriell:GM04729,
Wikidata:Q54838659
CVCL_Y882 2026-07-25 04:33:01 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 2026-07-25 04:33:00 1
GM04707
 
Resource Report
Resource Website
Coriell Cat# GM04707, RRID:CVCL_1I25 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Female GM04707A Coriell GM04707 CLO:CLO_0019024,
Coriell:GM04707,
Wikidata:Q54838641
CVCL_1I25 2026-07-25 04:33:01 0
GM04643
 
Resource Report
Resource Website
Coriell Cat# GM04643, RRID:CVCL_AA32 Homo sapiens (Human) Population: Caucasian. Finite cell line Female Coriell GM04643 CLO:CLO_0018965,
BioSample:SAMN00795436,
Coriell:GM04643,
Wikidata:Q54838617
CVCL_AA32 2026-07-25 04:33:00 0
GM04722
 
Resource Report
Resource Website
RRID:CVCL_Y870 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Female GM04722A CLO:CLO_0019075,
Coriell:GM04722,
Wikidata:Q54838654
CVCL_Y870 2026-07-25 04:33:01 0
GM04691
 
Resource Report
Resource Website
RRID:CVCL_1I22 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Male CLO:CLO_0019028,
Coriell:GM04691,
Wikidata:Q54838633
CVCL_1I22 2026-07-25 04:33:00 0
GM04614
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM04614, RRID:CVCL_V474 Homo sapiens (Human) Down syndrome PMID:6661932 Finite cell line Female GM 4614 Coriell GM04614 CLO:CLO_0018905,
Coriell:GM04614,
Wikidata:Q54838600
CVCL_V474 2026-07-25 04:33:00 0
GM04720
 
Resource Report
Resource Website
RRID:CVCL_0I33 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Female GM04720A CLO:CLO_0019077,
Coriell:GM04720,
Wikidata:Q54838652
CVCL_0I33 2026-07-25 04:33:01 0
GM04723
 
Resource Report
Resource Website
RRID:CVCL_Y871 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Female CLO:CLO_0019072,
Coriell:GM04723,
Wikidata:Q54838655
CVCL_Y871 2026-07-25 04:33:01 0
GM04617
 
Resource Report
Resource Website
RRID:CVCL_V476 Homo sapiens (Human) Down syndrome Karyotypic information: 47,XX,+21[25].arr(21)x3 (Coriell=GM04617)., Population: Puerto Rican. PMID:6661932 Finite cell line Female GM 4617 CLO:CLO_0018953,
Coriell:GM04617,
Wikidata:Q54838602
CVCL_V476 2026-07-25 04:33:00 0
GM04666
 
Resource Report
Resource Website
Coriell Cat# GM04666, RRID:CVCL_8A01 Homo sapiens (Human) Tourette syndrome Population: Caucasian. Finite cell line Female Coriell GM04666 CLO:CLO_0019009,
Coriell:GM04666,
Wikidata:Q54838623
CVCL_8A01 2026-07-25 04:33:00 0
GM04624
 
Resource Report
Resource Website
Coriell Cat# GM04624, RRID:CVCL_AA27 Homo sapiens (Human) Population: Native North American. Finite cell line Male Coriell GM04624 CLO:CLO_0018938,
Coriell:GM04624,
Wikidata:Q54838607
CVCL_AA27 2026-07-25 04:33:00 0
GM04681
 
Resource Report
Resource Website
RRID:CVCL_AT05 Homo sapiens (Human) Multiple sulfatase deficiency disease Population: Caucasian. PMID:6132606 Finite cell line Male GM 4681 CLO:CLO_0019037,
Coriell:GM04681,
Wikidata:Q54838627
CVCL_AT05 2026-07-25 04:33:00 0
GM04730
 
Resource Report
Resource Website
RRID:CVCL_Y883 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Female GM04730A CLO:CLO_0019068,
Coriell:GM04730,
Wikidata:Q54838660
CVCL_Y883 2026-07-25 04:33:01 0

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