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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
DD2912
 
Resource Report
Resource Website
ECACC Cat# 97052204, RRID:CVCL_9L54 Homo sapiens (Human) Karyotypic information: 46,XX,t(8;16)(q22;q13)mat (ECACC=97052204)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 97052204 ECACC:97052204,
Wikidata:Q54830464
CVCL_9L54 2026-08-15 04:26:57 0
DD2944
 
Resource Report
Resource Website
ECACC Cat# 97071618, RRID:CVCL_9L69 Homo sapiens (Human) Chondrodysplasia punctata Part of: ECACC chromosomal abnormality collection. Finite cell line Sex unspecified ECACC 97071618 ECACC:97071618,
Wikidata:Q54830485
CVCL_9L69 2026-08-15 04:26:57 0
DD2876
 
Resource Report
Resource Website
RRID:CVCL_9L40 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:97040608,
Wikidata:Q54830449
CVCL_9L40 2026-08-15 04:26:57 0
DD2897
 
Resource Report
Resource Website
ECACC Cat# 97043013, RRID:CVCL_9L49 Homo sapiens (Human) Karyotypic information: 46,XX,der(5,7)t(4;5;7)(q31:p13;q13:q21)mat (ECACC=97043013)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 97043013 ECACC:97043013,
Wikidata:Q54830459
CVCL_9L49 2026-08-15 04:26:57 0
DD2925
 
Resource Report
Resource Website
ECACC Cat# 97061820, RRID:CVCL_9L60 Homo sapiens (Human) Osteogenesis imperfecta Karyotypic information: 46,XY,dup(17)(q25.1;q25.3) (ECACC=97061820)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 97061820 ECACC:97061820,
Wikidata:Q54830472
CVCL_9L60 2026-08-15 04:26:57 0
DD2923
 
Resource Report
Resource Website
RRID:CVCL_9L59 Homo sapiens (Human) Karyotypic information: 46,XY,del(10)(qter->p15.1); de novo (ECACC=97061003)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC:97061003,
Wikidata:Q54830470
CVCL_9L59 2026-08-15 04:26:57 0
DD2913
 
Resource Report
Resource Website
RRID:CVCL_9L55 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:97052205,
Wikidata:Q54830465
CVCL_9L55 2026-08-15 04:26:57 0
DD2941
 
Resource Report
Resource Website
ECACC Cat# 97071615, RRID:CVCL_9L67 Homo sapiens (Human) Karyotypic information: 46,XY,dup(11)(p15.1;p15.3) (ECACC=97071615)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 97071615 ECACC:97071615,
Wikidata:Q54830483
CVCL_9L67 2026-08-15 04:26:57 0
DD2898
 
Resource Report
Resource Website
ECACC Cat# 97043014, RRID:CVCL_9L50 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 97043014 ECACC:97043014,
Wikidata:Q54830460
CVCL_9L50 2026-08-15 04:26:57 0
DD2913
 
Resource Report
Resource Website
ECACC Cat# 97052205, RRID:CVCL_9L55 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 97052205 ECACC:97052205,
Wikidata:Q54830465
CVCL_9L55 2026-08-15 04:26:57 0
DD2878
 
Resource Report
Resource Website
ECACC Cat# 97041117, RRID:CVCL_9L41 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 97041117 ECACC:97041117,
Wikidata:Q54830450
CVCL_9L41 2026-08-15 04:26:57 0
DD2939
 
Resource Report
Resource Website
RRID:CVCL_9L66 Homo sapiens (Human) Karyotypic information: 46,XX,add(2)(q37.3) (ECACC=97071613)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:97071613,
Wikidata:Q54830479
CVCL_9L66 2026-08-15 04:26:57 0
DD2863
 
Resource Report
Resource Website
ECACC Cat# 97030901, RRID:CVCL_9L32 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 97030901 ECACC:97030901,
Wikidata:Q54830437
CVCL_9L32 2026-08-15 04:26:56 0
DD2876
 
Resource Report
Resource Website
ECACC Cat# 97040608, RRID:CVCL_9L40 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 97040608 ECACC:97040608,
Wikidata:Q54830449
CVCL_9L40 2026-08-15 04:26:57 0
DD2904
 
Resource Report
Resource Website
ECACC Cat# 97051109, RRID:CVCL_9L52 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 97051109 ECACC:97051109,
Wikidata:Q54830462
CVCL_9L52 2026-08-15 04:26:57 0
DD2866
 
Resource Report
Resource Website
ECACC Cat# 97031403, RRID:CVCL_9L33 Homo sapiens (Human) Karyotypic information: 46,XY,der(15)t(10;15)(p11;p11)mat (ECACC=97031403)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 97031403 ECACC:97031403,
Wikidata:Q54830441
CVCL_9L33 2026-08-15 04:26:56 0
DD2893
 
Resource Report
Resource Website
ECACC Cat# 97042212, RRID:CVCL_AR36 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Sex unspecified ECACC 97042212 ECACC:97042212,
Wikidata:Q54830457
CVCL_AR36 2026-08-15 04:26:57 0
DD2922
 
Resource Report
Resource Website
RRID:CVCL_9L58 Homo sapiens (Human) Karyotypic information: 46,XX,del(5)(p1?3.3;p14.2)pat (ECACC=97061002)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:97061002,
Wikidata:Q54830469
CVCL_9L58 2026-08-15 04:26:57 0
DD2880
 
Resource Report
Resource Website
ECACC Cat# 97040923, RRID:CVCL_9L42 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 97040923 ECACC:97040923,
Wikidata:Q54830451
CVCL_9L42 2026-08-15 04:26:57 0
DD2868
 
Resource Report
Resource Website
RRID:CVCL_9L35 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:97031817,
Wikidata:Q54830443
CVCL_9L35 2026-08-15 04:26:56 0

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