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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
DD3041
 
Resource Report
Resource Website
ECACC Cat# 98011601, RRID:CVCL_9M00 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 98011601 ECACC:98011601,
Wikidata:Q54830533
CVCL_9M00 2026-08-15 04:26:59 0
DD3004
 
Resource Report
Resource Website
RRID:CVCL_9L87 Homo sapiens (Human) Karyotypic information: 47,XX,+mar.ish der(22)(D22Z3+) (ECACC=97110612)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC:97110612,
Wikidata:Q54830510
CVCL_9L87 2026-08-15 04:26:59 0
DD3023
 
Resource Report
Resource Website
ECACC Cat# 97121102, RRID:CVCL_9L94 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 97121102 ECACC:97121102,
Wikidata:Q54830518
CVCL_9L94 2026-08-15 04:26:58 0
DD2958
 
Resource Report
Resource Website
ECACC Cat# 97080402, RRID:CVCL_9L74 Homo sapiens (Human) Karyotypic information: 46,XY,t(17;20)(p13.3;q13.31) (ECACC=97080402)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 97080402 ECACC:97080402,
Wikidata:Q54830490
CVCL_9L74 2026-08-15 04:26:58 0
DD2969
 
Resource Report
Resource Website
ECACC Cat# 97082210, RRID:CVCL_9L76 Homo sapiens (Human) Wilms tumor Karyotypic information: 46,XY,del(12)(q11.2;q13.11) (ECACC=97082210)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 97082210 ECACC:97082210,
Wikidata:Q54830493
CVCL_9L76 2026-08-15 04:26:58 0
DD3006
 
Resource Report
Resource Website
ECACC Cat# 97110614, RRID:CVCL_9L88 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 97110614 ECACC:97110614,
Wikidata:Q54830512
CVCL_9L88 2026-08-15 04:26:58 0
DD3028
 
Resource Report
Resource Website
RRID:CVCL_9N71 Homo sapiens (Human) Developmental delay Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:97122203,
Wikidata:Q54830526
CVCL_9N71 2026-08-15 04:26:58 0
DD3011
 
Resource Report
Resource Website
RRID:CVCL_9L90 Homo sapiens (Human) Karyotypic information: 46,XX,t(9;20)(p24.1;p11.2?3) (ECACC=97112202)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:97112202,
Wikidata:Q54830514
CVCL_9L90 2026-08-15 04:26:58 0
DD2968
 
Resource Report
Resource Website
RRID:CVCL_9L75 Homo sapiens (Human) Karyotypic information: 46,X,del(X)(p22.13;p22.31) (ECACC=97082209)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:97082209,
Wikidata:Q54830492
CVCL_9L75 2026-08-15 04:26:58 0
DD3034
 
Resource Report
Resource Website
RRID:CVCL_9L98 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:98010202,
Wikidata:Q54830531
CVCL_9L98 2026-08-15 04:26:59 0
DD2977
 
Resource Report
Resource Website
RRID:CVCL_9L79 Homo sapiens (Human) Autism spectrum disorder Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:97091131,
Wikidata:Q54830496
CVCL_9L79 2026-08-15 04:26:58 0
DD2976
 
Resource Report
Resource Website
ECACC Cat# 97091130, RRID:CVCL_9L78 Homo sapiens (Human) Karyotypic information: 46,XY,inv(14)(q24.11;q32.1)pat (ECACC=97091130)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 97091130 ECACC:97091130,
Wikidata:Q54830495
CVCL_9L78 2026-08-15 04:26:58 0
DD2987
 
Resource Report
Resource Website
ECACC Cat# 97100307, RRID:CVCL_AR40 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 97100307 ECACC:97100307,
Wikidata:Q54830500
CVCL_AR40 2026-08-15 04:26:58 0
DD3025
 
Resource Report
Resource Website
RRID:CVCL_9N68 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:97121508,
Wikidata:Q54830520
CVCL_9N68 2026-08-15 04:26:58 0
DD2986
 
Resource Report
Resource Website
RRID:CVCL_AR39 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:97100212,
Wikidata:Q54830499
CVCL_AR39 2026-08-15 04:26:58 0
DD3067
 
Resource Report
Resource Website
RRID:CVCL_9M05 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:98030405,
Wikidata:Q54830540
CVCL_9M05 2026-08-15 04:26:59 0
DD3041
 
Resource Report
Resource Website
RRID:CVCL_9M00 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:98011601,
Wikidata:Q54830533
CVCL_9M00 2026-08-15 04:26:59 0
DD3066
 
Resource Report
Resource Website
RRID:CVCL_9M04 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC:98030404,
Wikidata:Q54830539
CVCL_9M04 2026-08-15 04:26:59 0
DD3045
 
Resource Report
Resource Website
RRID:CVCL_9N74 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:98011911,
Wikidata:Q54830535
CVCL_9N74 2026-08-15 04:26:59 0
DD3027
 
Resource Report
Resource Website
RRID:CVCL_9N70 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:97121905,
Wikidata:Q54830522
CVCL_9N70 2026-08-15 04:26:59 0

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