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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
DD2301
 
Resource Report
Resource Website
ECACC Cat# 95060908, RRID:CVCL_9J52 Homo sapiens (Human) Karyotypic information: 46,XY,-13,+der(13),t(Y;13)(q12;p11)mat (ECACC=95060908)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 95060908 ECACC:95060908,
Wikidata:Q54830201
CVCL_9J52 2026-08-15 04:26:49 0
DD2253
 
Resource Report
Resource Website
RRID:CVCL_9J37 Homo sapiens (Human) Karyotypic information: 46,XX,del(9)(qter->p22) (ECACC=95041308)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:95041308,
Wikidata:Q54830184
CVCL_9J37 2026-08-15 04:26:52 0
DD2221
 
Resource Report
Resource Website
RRID:CVCL_AQ91 Homo sapiens (Human) Karyotypic information: 46,XY; 47,XY,+7 (ECACC=95030626)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC:95030626,
Wikidata:Q54830169
CVCL_AQ91 2026-08-15 04:26:51 0
DD2264
 
Resource Report
Resource Website
ECACC Cat# 95050520, RRID:CVCL_AQ94 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 95050520 ECACC:95050520,
Wikidata:Q54830189
CVCL_AQ94 2026-08-15 04:26:49 0
DD2323
 
Resource Report
Resource Website
RRID:CVCL_9J64 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:95061613,
Wikidata:Q54830214
CVCL_9J64 2026-08-15 04:26:53 0
DD2261
 
Resource Report
Resource Website
RRID:CVCL_9J41 Homo sapiens (Human) Trisomy 18 Karyotypic information: 47,XX,+18 (ECACC=95050105)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC:95050105,
Wikidata:Q54830188
CVCL_9J41 2026-08-15 04:26:49 0
DD2281
 
Resource Report
Resource Website
RRID:CVCL_9J45 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:95053002,
Wikidata:Q54830194
CVCL_9J45 2026-08-15 04:26:49 0
DD2208
 
Resource Report
Resource Website
RRID:CVCL_9J26 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC:95021603,
Wikidata:Q54830166
CVCL_9J26 2026-08-15 04:26:51 0
DD2291
 
Resource Report
Resource Website
RRID:CVCL_9J49 Homo sapiens (Human) Smith-Magenis syndrome Karyotypic information: 46,XY,del(17)(p11.2;p11.2) (ECACC=95060215)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC:95060215,
Wikidata:Q54830198
CVCL_9J49 2026-08-15 04:26:49 0
DD2323
 
Resource Report
Resource Website
ECACC Cat# 95061613, RRID:CVCL_9J64 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 95061613 ECACC:95061613,
Wikidata:Q54830214
CVCL_9J64 2026-08-15 04:26:50 0
DD2260
 
Resource Report
Resource Website
ECACC Cat# 95050104, RRID:CVCL_9J40 Homo sapiens (Human) Trisomy 13 Karyotypic information: 47,XX,+13 (ECACC=95050104)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 95050104 ECACC:95050104,
Wikidata:Q54830187
CVCL_9J40 2026-08-15 04:26:49 0
DD2393
 
Resource Report
Resource Website
RRID:CVCL_9J95 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Finite cell line Sex ambiguous ECACC:95080801,
Wikidata:Q54830252
CVCL_9J95 2026-08-15 04:26:51 0
DD2363
 
Resource Report
Resource Website
RRID:CVCL_9J91 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:95070103,
Wikidata:Q54830247
CVCL_9J91 2026-08-15 04:26:51 0
DD2341
 
Resource Report
Resource Website
RRID:CVCL_AQ98 Homo sapiens (Human) Karyotypic information: 46,XX.ish:22q11.2(cH748x22) (ECACC=95062316)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC:95062316,
Wikidata:Q54830232
CVCL_AQ98 2026-08-15 04:26:50 0
DD2422
 
Resource Report
Resource Website
ECACC Cat# 95091603, RRID:CVCL_9K02 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 95091603 ECACC:95091603,
Wikidata:Q54830262
CVCL_9K02 2026-08-15 04:26:51 0
DD2388
 
Resource Report
Resource Website
ECACC Cat# 95072401, RRID:CVCL_AQ99 Homo sapiens (Human) Trisomy 21 Karyotypic information: 47,XY,+21 (ECACC=95072401)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 95072401 ECACC:95072401,
Wikidata:Q54830249
CVCL_AQ99 2026-08-15 04:26:54 0
DD2340
 
Resource Report
Resource Website
ECACC Cat# 95062315, RRID:CVCL_9J76 Homo sapiens (Human) Karyotypic information: 47,XY,+psu dic(15)(pter->q12::q12->pter) (ECACC=95062315)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 95062315 ECACC:95062315,
Wikidata:Q54830231
CVCL_9J76 2026-08-15 04:26:53 0
DD2349
 
Resource Report
Resource Website
ECACC Cat# 95062820, RRID:CVCL_9J82 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 95062820 ECACC:95062820,
Wikidata:Q54830238
CVCL_9J82 2026-08-15 04:26:50 0
DD2450
 
Resource Report
Resource Website
RRID:CVCL_9K06 Homo sapiens (Human) Karyotypic information: 46,XX,-7,+der(7),t(7;19)(q36.1;q13.43)pat (ECACC=95103002)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC:95103002,
Wikidata:Q54830268
CVCL_9K06 2026-08-15 04:26:51 0
DD2422
 
Resource Report
Resource Website
RRID:CVCL_9K02 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:95091603,
Wikidata:Q54830262
CVCL_9K02 2026-08-15 04:26:51 0

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