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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
DD0132
 
Resource Report
Resource Website
RRID:CVCL_8U80 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:91010402,
Wikidata:Q54828768
CVCL_8U80 2026-08-15 04:26:11 0
DD0084
 
Resource Report
Resource Website
ECACC Cat# 90020901, RRID:CVCL_8U61 Homo sapiens (Human) Pallister-Killian syndrome Karyotypic information: 46,XY; 47,XY,+i(12p) (ECACC=90020901)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 90020901 ECACC:90020901,
Wikidata:Q54828746
CVCL_8U61 2026-08-15 04:26:11 0
DD0122
 
Resource Report
Resource Website
ECACC Cat# 90121814, RRID:CVCL_8U76 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 90121814 ECACC:90121814,
Wikidata:Q54828764
CVCL_8U76 2026-08-15 04:26:11 0
DD0097
 
Resource Report
Resource Website
ECACC Cat# 89082301, RRID:CVCL_8U65 Homo sapiens (Human) Karyotypic information: 46,XX,-4,+der(4)t(X;4)(p22.1;p15.2); de novo (ECACC=89082301)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 89082301 ECACC:89082301,
Wikidata:Q54828750
CVCL_8U65 2026-08-15 04:26:12 0
DD0104
 
Resource Report
Resource Website
RRID:CVCL_8U70 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC:88122801,
Wikidata:Q54828756
CVCL_8U70 2026-08-15 04:26:12 0
DD0099
 
Resource Report
Resource Website
ECACC Cat# 89060701, RRID:CVCL_8U67 Homo sapiens (Human) Karyotypic information: 46,X,t(X;9)(p21.2;q22.1); de novo (ECACC=89060701)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 89060701 ECACC:89060701,
Wikidata:Q54828752
CVCL_8U67 2026-08-15 04:26:11 0
DD0033
 
Resource Report
Resource Website
ECACC Cat# 90092604, RRID:CVCL_8U42 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 90092604 ECACC:90092604,
Wikidata:Q54828720
CVCL_8U42 2026-08-15 04:26:10 0
DD0143
 
Resource Report
Resource Website
RRID:CVCL_8U86 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:91011607,
Wikidata:Q54828775
CVCL_8U86 2026-08-15 04:26:12 0
DD0086
 
Resource Report
Resource Website
RRID:CVCL_8U63 Homo sapiens (Human) Karyotypic information: 46,XX; 46,XX,t(2;11) (ECACC=90010302)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC:90010302,
Wikidata:Q54828748
CVCL_8U63 2026-08-15 04:26:11 0
DD0133
 
Resource Report
Resource Website
RRID:CVCL_8U81 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC:91010902,
Wikidata:Q54828769
CVCL_8U81 2026-08-15 04:26:11 0
DD0132
 
Resource Report
Resource Website
ECACC Cat# 91010402, RRID:CVCL_8U80 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 91010402 ECACC:91010402,
Wikidata:Q54828768
CVCL_8U80 2026-08-15 04:26:13 0
DD0136
 
Resource Report
Resource Website
ECACC Cat# 91011104, RRID:CVCL_8U82 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 91011104 ECACC:91011104,
Wikidata:Q54828770
CVCL_8U82 2026-08-15 04:26:11 0
DD0051
 
Resource Report
Resource Website
RRID:CVCL_8U51 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC:90110201,
Wikidata:Q54828732
CVCL_8U51 2026-08-15 04:26:10 0
DD0144
 
Resource Report
Resource Website
ECACC Cat# 91011608, RRID:CVCL_8U87 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 91011608 ECACC:91011608,
Wikidata:Q54828776
CVCL_8U87 2026-08-15 04:26:12 0
DD0058
 
Resource Report
Resource Website
RRID:CVCL_8U55 Homo sapiens (Human) Fragile X syndrome Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC:90090604,
Wikidata:Q54828740
CVCL_8U55 2026-08-15 04:26:12 0
DD0031
 
Resource Report
Resource Website
ECACC Cat# 90091201, RRID:CVCL_8U41 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 90091201 ECACC:90091201,
Wikidata:Q54828719
CVCL_8U41 2026-08-15 04:26:10 0
DD0105
 
Resource Report
Resource Website
RRID:CVCL_8U71 Homo sapiens (Human) Methylmalonic acidemia Karyotypic information: 46,XY,fra(X)(q28) 16/50 (ECACC=88101401)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC:88101401,
Wikidata:Q54828758
CVCL_8U71 2026-08-15 04:26:11 0
DD0126
 
Resource Report
Resource Website
ECACC Cat# 90122403, RRID:CVCL_8U77 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 90122403 ECACC:90122403,
Wikidata:Q54828765
CVCL_8U77 2026-08-15 04:26:13 0
DD0037
 
Resource Report
Resource Website
RRID:CVCL_8U45 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:90092709,
Wikidata:Q54828723
CVCL_8U45 2026-08-15 04:26:12 0
DD0128
 
Resource Report
Resource Website
ECACC Cat# 90122405, RRID:CVCL_8U79 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 90122405 ECACC:90122405,
Wikidata:Q54828767
CVCL_8U79 2026-08-15 04:26:11 0

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