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6,967 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
DD0724
 
Resource Report
Resource Website
ECACC Cat# 92042410, RRID:CVCL_9B62 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92042410 ECACC:92042410,
Wikidata:Q54829218
CVCL_9B62 2026-08-08 04:56:52 0
DD0759
 
Resource Report
Resource Website
ECACC Cat# 92051804, RRID:CVCL_9B88 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92051804 ECACC:92051804,
Wikidata:Q54829261
CVCL_9B88 2026-08-08 04:56:53 0
DD0772
 
Resource Report
Resource Website
ECACC Cat# 92052213, RRID:CVCL_9B99 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92052213 ECACC:92052213,
Wikidata:Q54829274
CVCL_9B99 2026-08-08 04:56:54 0
DD0740
 
Resource Report
Resource Website
ECACC Cat# 92043036, RRID:CVCL_9B74 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92043036 ECACC:92043036,
Wikidata:Q54829243
CVCL_9B74 2026-08-08 04:56:53 0
DD0801
 
Resource Report
Resource Website
ECACC Cat# 92061217, RRID:CVCL_9C22 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92061217 ECACC:92061217,
Wikidata:Q54829327
CVCL_9C22 2026-08-08 04:56:54 0
DD0808
 
Resource Report
Resource Website
ECACC Cat# 92061505, RRID:CVCL_9C28 Homo sapiens (Human) 47,XYY syndrome Karyotypic information: 46,XY; 47,XYY (ECACC=92061505)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92061505 ECACC:92061505,
Wikidata:Q54829334
CVCL_9C28 2026-08-08 04:56:54 0
DD0781
 
Resource Report
Resource Website
ECACC Cat# 92060310, RRID:CVCL_9C06 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92060310 ECACC:92060310,
Wikidata:Q54829282
CVCL_9C06 2026-08-08 04:56:54 0
DD0789
 
Resource Report
Resource Website
ECACC Cat# 92060527, RRID:CVCL_9C13 Homo sapiens (Human) Karyotypic information: 47,XX,+dic(15)(pter->q11::q11->pter) (ECACC=92060527)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92060527 ECACC:92060527,
Wikidata:Q54829316
CVCL_9C13 2026-08-08 04:56:54 0
DD0787
 
Resource Report
Resource Website
ECACC Cat# 92060502, RRID:CVCL_9C11 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92060502 ECACC:92060502,
Wikidata:Q54829288
CVCL_9C11 2026-08-08 04:56:54 0
DD0784
 
Resource Report
Resource Website
ECACC Cat# 92060313, RRID:CVCL_9C09 Homo sapiens (Human) Fragile X syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92060313 ECACC:92060313,
Wikidata:Q54829285
CVCL_9C09 2026-08-08 04:56:54 0
DD0827
 
Resource Report
Resource Website
ECACC Cat# 92062583, RRID:CVCL_9C45 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92062583 ECACC:92062583,
Wikidata:Q54829354
CVCL_9C45 2026-08-08 04:56:55 0
DD0826
 
Resource Report
Resource Website
ECACC Cat# 92062582, RRID:CVCL_9C44 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92062582 ECACC:92062582,
Wikidata:Q54829353
CVCL_9C44 2026-08-08 04:56:55 0
DD0782
 
Resource Report
Resource Website
ECACC Cat# 92060311, RRID:CVCL_9C07 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92060311 ECACC:92060311,
Wikidata:Q54829283
CVCL_9C07 2026-08-08 04:56:54 0
DD0819
 
Resource Report
Resource Website
ECACC Cat# 92062575, RRID:CVCL_9C37 Homo sapiens (Human) Karyotypic information: 46,XY,t(9;15)(q22;q13)(?O) (ECACC=92062575)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92062575 ECACC:92062575,
Wikidata:Q54829345
CVCL_9C37 2026-08-08 04:56:54 0
DD0813
 
Resource Report
Resource Website
ECACC Cat# 92062318, RRID:CVCL_9C33 Homo sapiens (Human) Karyotypic information: 46,XY,19q+ (ECACC=92062318)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92062318 ECACC:92062318,
Wikidata:Q54829340
CVCL_9C33 2026-08-08 04:56:54 0
DD0800
 
Resource Report
Resource Website
ECACC Cat# 92061216, RRID:CVCL_9C21 Homo sapiens (Human) Klinefelter syndrome Karyotypic information: 47,XXY (ECACC=92061216)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92061216 ECACC:92061216,
Wikidata:Q54829326
CVCL_9C21 2026-08-08 04:56:54 0
DD0834
 
Resource Report
Resource Website
ECACC Cat# 92070113, RRID:CVCL_9C50 Homo sapiens (Human) Trisomy 18 Karyotypic information: 47,XY,+18 (ECACC=92070113)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 92070113 ECACC:92070113,
Wikidata:Q54829360
CVCL_9C50 2026-08-08 04:56:55 0
DD0793
 
Resource Report
Resource Website
ECACC Cat# 92060903, RRID:CVCL_9C15 Homo sapiens (Human) Karyotypic information: 46,XX,t(12;22)(12p22p;12q22q)mat (ECACC=92060903)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92060903 ECACC:92060903,
Wikidata:Q54829319
CVCL_9C15 2026-08-08 04:56:54 0
DD0807
 
Resource Report
Resource Website
ECACC Cat# 92061504, RRID:CVCL_9C27 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92061504 ECACC:92061504,
Wikidata:Q54829333
CVCL_9C27 2026-08-08 04:56:54 0
DD0802
 
Resource Report
Resource Website
ECACC Cat# 92061218, RRID:CVCL_9C23 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92061218 ECACC:92061218,
Wikidata:Q54829328
CVCL_9C23 2026-08-08 04:56:54 0

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