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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
DD0655
 
Resource Report
Resource Website
ECACC Cat# 92030301, RRID:CVCL_9B25 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92030301 ECACC:92030301,
Wikidata:Q54829173
CVCL_9B25 2026-08-29 04:24:44 0
DD0705
 
Resource Report
Resource Website
ECACC Cat# 92041418, RRID:CVCL_9B51 Homo sapiens (Human) Karyotypic information: 46,XY,del(20)(p11.21;p11.23); de novo (ECACC=92041418)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92041418 ECACC:92041418,
Wikidata:Q54829207
CVCL_9B51 2026-08-29 04:24:44 0
DD0646
 
Resource Report
Resource Website
ECACC Cat# 92022803, RRID:CVCL_9B17 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92022803 ECACC:92022803,
Wikidata:Q54829164
CVCL_9B17 2026-08-29 04:24:46 0
DD0677
 
Resource Report
Resource Website
ECACC Cat# 92031805, RRID:CVCL_9B38 Homo sapiens (Human) Trisomy 18 Karyotypic information: 47,XY,+18 (ECACC=92031805)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 92031805 ECACC:92031805,
Wikidata:Q54829194
CVCL_9B38 2026-08-29 04:24:46 0
DD0635
 
Resource Report
Resource Website
ECACC Cat# 92021925, RRID:CVCL_9B11 Homo sapiens (Human) Trisomy 18 Karyotypic information: 47,XX,+18 (ECACC=92021925)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 92021925 ECACC:92021925,
Wikidata:Q54829158
CVCL_9B11 2026-08-29 04:24:46 0
DD0711
 
Resource Report
Resource Website
ECACC Cat# 92042109, RRID:CVCL_9B56 Homo sapiens (Human) Congenital hydrocephalus Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 92042109 ECACC:92042109,
Wikidata:Q54829212
CVCL_9B56 2026-08-29 04:24:47 0
DD0650
 
Resource Report
Resource Website
ECACC Cat# 92022807, RRID:CVCL_9B21 Homo sapiens (Human) Wolf-Hirschhorn syndrome Karyotypic information: 46,XY,-4,+?der(4)(qter->p16;?) (ECACC=92022807)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92022807 ECACC:92022807,
Wikidata:Q54829169
CVCL_9B21 2026-08-29 04:24:44 0
DD0632
 
Resource Report
Resource Website
ECACC Cat# 92021922, RRID:CVCL_9B09 Homo sapiens (Human) Karyotypic information: 46,XX,del(1)(pter->q43)(?0) (ECACC=92021922)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92021922 ECACC:92021922,
Wikidata:Q54829156
CVCL_9B09 2026-08-29 04:24:43 0
DD0670
 
Resource Report
Resource Website
ECACC Cat# 92030647, RRID:CVCL_9B32 Homo sapiens (Human) Hydrops fetalis Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 92030647 ECACC:92030647,
Wikidata:Q54829180
CVCL_9B32 2026-08-29 04:24:46 0
DD0651
 
Resource Report
Resource Website
ECACC Cat# 92022808, RRID:CVCL_9B22 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92022808 ECACC:92022808,
Wikidata:Q54829170
CVCL_9B22 2026-08-29 04:24:44 0
DD0689
 
Resource Report
Resource Website
ECACC Cat# 92033007, RRID:CVCL_9B44 Homo sapiens (Human) Congenital hydrocephalus Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 92033007 ECACC:92033007,
Wikidata:Q54829200
CVCL_9B44 2026-08-29 04:24:46 0
DD0698
 
Resource Report
Resource Website
ECACC Cat# 92040904, RRID:CVCL_9B47 Homo sapiens (Human) Klinefelter syndrome Karyotypic information: 47,XXY (ECACC=92040904)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92040904 ECACC:92040904,
Wikidata:Q54829203
CVCL_9B47 2026-08-29 04:24:46 0
DD0693
 
Resource Report
Resource Website
ECACC Cat# 92040308, RRID:CVCL_9B45 Homo sapiens (Human) Karyotypic information: 46,XX,t(13;18)(q22;q21.3)(?O) (ECACC=92040308)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92040308 ECACC:92040308,
Wikidata:Q54829201
CVCL_9B45 2026-08-29 04:24:44 0
DD0696
 
Resource Report
Resource Website
ECACC Cat# 92040902, RRID:CVCL_9B46 Homo sapiens (Human) Karyotypic information: 46,XX,del(18)(pter->q21.1); de novo (ECACC=92040902)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 92040902 ECACC:92040902,
Wikidata:Q54829202
CVCL_9B46 2026-08-29 04:24:44 0
DD0665
 
Resource Report
Resource Website
ECACC Cat# 92030642, RRID:CVCL_9B29 Homo sapiens (Human) Karyotypic information: 46,XY,t(1;13)(p22;q32)(?O) (ECACC=92030642)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92030642 ECACC:92030642,
Wikidata:Q54829177
CVCL_9B29 2026-08-29 04:24:46 0
DD0664
 
Resource Report
Resource Website
ECACC Cat# 92030625, RRID:CVCL_9B28 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92030625 ECACC:92030625,
Wikidata:Q54829176
CVCL_9B28 2026-08-29 04:24:44 0
DD0671
 
Resource Report
Resource Website
ECACC Cat# 92031101, RRID:CVCL_9B33 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92031101 ECACC:92031101,
Wikidata:Q54829188
CVCL_9B33 2026-08-29 04:24:44 0
DD0649
 
Resource Report
Resource Website
ECACC Cat# 92022806, RRID:CVCL_9B20 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92022806 ECACC:92022806,
Wikidata:Q54829168
CVCL_9B20 2026-08-29 04:24:46 0
DD0667
 
Resource Report
Resource Website
ECACC Cat# 92030644, RRID:CVCL_9B31 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92030644 ECACC:92030644,
Wikidata:Q54829179
CVCL_9B31 2026-08-29 04:24:44 0
DD0638
 
Resource Report
Resource Website
ECACC Cat# 92022114, RRID:CVCL_9B14 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92022114 ECACC:92022114,
Wikidata:Q54829161
CVCL_9B14 2026-08-29 04:24:46 0

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