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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
DD3204
 
Resource Report
Resource Website
RRID:CVCL_9N83 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC:98072204,
Wikidata:Q54830612
CVCL_9N83 2026-08-15 04:27:01 0
DD3236
 
Resource Report
Resource Website
RRID:CVCL_9M69 Homo sapiens (Human) Karyotypic information: 46,XY,?dup(5)(p14.2;p15.1) (ECACC=98090102)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC:98090102,
Wikidata:Q54830628
CVCL_9M69 2026-08-15 04:27:01 0
DD3207
 
Resource Report
Resource Website
RRID:CVCL_9M65 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Finite cell line Sex unspecified ECACC:98072412,
Wikidata:Q54830614
CVCL_9M65 2026-08-15 04:27:02 0
DD3263
 
Resource Report
Resource Website
ECACC Cat# 98102401, RRID:CVCL_9M75 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 98102401 ECACC:98102401,
Wikidata:Q54830646
CVCL_9M75 2026-08-15 04:27:02 0
DD3201
 
Resource Report
Resource Website
RRID:CVCL_9M61 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC:98072104,
Wikidata:Q54830607
CVCL_9M61 2026-08-15 04:27:01 0
DD3175
 
Resource Report
Resource Website
ECACC Cat# 98062508, RRID:CVCL_9M52 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 98062508 ECACC:98062508,
Wikidata:Q54830596
CVCL_9M52 2026-08-15 04:27:00 0
DD3230
 
Resource Report
Resource Website
ECACC Cat# 98082509, RRID:CVCL_9N93 Homo sapiens (Human) Karyotypic information: 46,XY,t(4;12)(q32.2;21.2)mat (ECACC=98082509)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 98082509 ECACC:98082509,
Wikidata:Q54830626
CVCL_9N93 2026-08-15 04:27:01 0
DD3244
 
Resource Report
Resource Website
RRID:CVCL_9N97 Homo sapiens (Human) Aortic valve stenosis Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC:98100710,
Wikidata:Q54830632
CVCL_9N97 2026-08-15 04:27:02 0
DD3230
 
Resource Report
Resource Website
RRID:CVCL_9N93 Homo sapiens (Human) Karyotypic information: 46,XY,t(4;12)(q32.2;21.2)mat (ECACC=98082509)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC:98082509,
Wikidata:Q54830626
CVCL_9N93 2026-08-15 04:27:02 0
DD3257
 
Resource Report
Resource Website
ECACC Cat# 98102002, RRID:CVCL_9M73 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 98102002 ECACC:98102002,
Wikidata:Q54830641
CVCL_9M73 2026-08-15 04:27:02 0
DD3177
 
Resource Report
Resource Website
RRID:CVCL_9M53 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:98062902,
Wikidata:Q54830597
CVCL_9M53 2026-08-15 04:27:01 0
DD3259
 
Resource Report
Resource Website
RRID:CVCL_9P03 Homo sapiens (Human) Karyotypic information: 46,XX,t(1;4)(q23;p15.3)mat (ECACC=98102201)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC:98102201,
Wikidata:Q54830642
CVCL_9P03 2026-08-15 04:27:02 0
DD3213
 
Resource Report
Resource Website
ECACC Cat# 98072907, RRID:CVCL_9N84 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 98072907 ECACC:98072907,
Wikidata:Q54830616
CVCL_9N84 2026-08-15 04:27:01 0
DD3186
 
Resource Report
Resource Website
ECACC Cat# 98071001, RRID:CVCL_9N82 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 98071001 ECACC:98071001,
Wikidata:Q54830599
CVCL_9N82 2026-08-15 04:27:00 0
DD3194
 
Resource Report
Resource Website
ECACC Cat# 98071705, RRID:CVCL_9M55 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 98071705 ECACC:98071705,
Wikidata:Q54830601
CVCL_9M55 2026-08-15 04:27:01 0
DD3215
 
Resource Report
Resource Website
RRID:CVCL_9N86 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC:98072909,
Wikidata:Q54830618
CVCL_9N86 2026-08-15 04:27:01 0
DD3186
 
Resource Report
Resource Website
RRID:CVCL_9N82 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:98071001,
Wikidata:Q54830599
CVCL_9N82 2026-08-15 04:27:00 0
DD3235
 
Resource Report
Resource Website
RRID:CVCL_9M68 Homo sapiens (Human) Karyotypic information: 46,XX,t(2;5)(q31.1;q23.2); de novo (ECACC=98090101)., Part of: ECACC chromosomal abnormality collection. PMID:15635069 Transformed cell line Female ECACC:98090101,
Wikidata:Q54830627
CVCL_9M68 2026-08-15 04:27:01 0
DD3249
 
Resource Report
Resource Website
ECACC Cat# 98100910, RRID:CVCL_9P01 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 98100910 ECACC:98100910,
Wikidata:Q54830636
CVCL_9P01 2026-08-15 04:27:02 0
DD3262
 
Resource Report
Resource Website
ECACC Cat# 98102204, RRID:CVCL_9M74 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 98102204 ECACC:98102204,
Wikidata:Q54830645
CVCL_9M74 2026-08-15 04:27:03 0

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