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  • Vendor:ecacc (facet)

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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
DD0102
 
Resource Report
Resource Website
ECACC Cat# 89021601, RRID:CVCL_8U69 Homo sapiens (Human) Fragile X syndrome Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 89021601 ECACC:89021601,
Wikidata:Q54828755
CVCL_8U69 2026-08-29 04:24:40 0
DD0100
 
Resource Report
Resource Website
ECACC Cat# 89031702, RRID:CVCL_8U68 Homo sapiens (Human) Methylmalonic acidemia Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 89031702 ECACC:89031702,
Wikidata:Q54828754
CVCL_8U68 2026-08-29 04:24:34 0
DD0034
 
Resource Report
Resource Website
ECACC Cat# 90092605, RRID:CVCL_8U43 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 90092605 ECACC:90092605,
Wikidata:Q54828721
CVCL_8U43 2026-08-29 04:24:33 0
DD0140
 
Resource Report
Resource Website
ECACC Cat# 91011103, RRID:CVCL_8U83 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 91011103 ECACC:91011103,
Wikidata:Q54828771
CVCL_8U83 2026-08-29 04:24:34 0
DD0086
 
Resource Report
Resource Website
ECACC Cat# 90010302, 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 ECACC:90010302,
Wikidata:Q54828748
CVCL_8U63 2026-08-29 04:24:40 0
DD0054
 
Resource Report
Resource Website
ECACC Cat# 90112722, RRID:CVCL_8U52 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 90112722 ECACC:90112722,
Wikidata:Q54828733
CVCL_8U52 2026-08-29 04:24:34 0
DD0041
 
Resource Report
Resource Website
ECACC Cat# 90100701, RRID:CVCL_8U47 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 90100701 ECACC:90100701,
Wikidata:Q54828726
CVCL_8U47 2026-08-29 04:24:33 0
DD0056
 
Resource Report
Resource Website
ECACC Cat# 90091701, RRID:CVCL_8U53 Homo sapiens (Human) Karyotypic information: 46,XY,t(4;9)(p16;q32)pat (ECACC=90091701)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 90091701 ECACC:90091701,
Wikidata:Q54828734
CVCL_8U53 2026-08-29 04:24:34 0
DD0133
 
Resource Report
Resource Website
ECACC Cat# 91010902, RRID:CVCL_8U81 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 91010902 ECACC:91010902,
Wikidata:Q54828769
CVCL_8U81 2026-08-29 04:24:40 0
DD0105
 
Resource Report
Resource Website
ECACC Cat# 88101401, 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 ECACC:88101401,
Wikidata:Q54828758
CVCL_8U71 2026-08-29 04:24:34 0
DD0038
 
Resource Report
Resource Website
ECACC Cat# 90092710, RRID:CVCL_8U46 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 90092710 ECACC:90092710,
Wikidata:Q54828724
CVCL_8U46 2026-08-29 04:24:33 0
DD0074
 
Resource Report
Resource Website
ECACC Cat# 90042502, RRID:CVCL_8U60 Homo sapiens (Human) Karyotypic information: 47,XX,+14 (ECACC=90042502)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 90042502 ECACC:90042502,
Wikidata:Q54828745
CVCL_8U60 2026-08-29 04:24:40 0
DD0127
 
Resource Report
Resource Website
ECACC Cat# 90122404, RRID:CVCL_8U78 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. PMID:15635069 Transformed cell line Female ECACC 90122404 ECACC:90122404,
Wikidata:Q54828766
CVCL_8U78 2026-08-29 04:24:40 0
DD0143
 
Resource Report
Resource Website
ECACC Cat# 91011607, RRID:CVCL_8U86 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 91011607 ECACC:91011607,
Wikidata:Q54828775
CVCL_8U86 2026-08-29 04:24:34 0
DD0049
 
Resource Report
Resource Website
ECACC Cat# 90102417, RRID:CVCL_8U50 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 90102417 ECACC:90102417,
Wikidata:Q54828731
CVCL_8U50 2026-08-29 04:24:33 0
DD0042
 
Resource Report
Resource Website
ECACC Cat# 90101001, RRID:CVCL_8U48 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 90101001 ECACC:90101001,
Wikidata:Q54828727
CVCL_8U48 2026-08-29 04:24:33 0
DD0120
 
Resource Report
Resource Website
ECACC Cat# 90121812, RRID:CVCL_8U75 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 90121812 ECACC:90121812,
Wikidata:Q54828762
CVCL_8U75 2026-08-29 04:24:40 0
DD0227
 
Resource Report
Resource Website
ECACC Cat# 91032717, RRID:CVCL_8V35 Homo sapiens (Human) Developmental delay Karyotypic information: 46,XY; 47,XY,+mar; de novo (ECACC=91032717)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 91032717 ECACC:91032717,
Wikidata:Q54828846
CVCL_8V35 2026-08-29 04:24:36 0
DD0183
 
Resource Report
Resource Website
ECACC Cat# 91022217, RRID:CVCL_8V05 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 91022217 ECACC:91022217,
Wikidata:Q54828805
CVCL_8V05 2026-08-29 04:24:35 0
DD0215
 
Resource Report
Resource Website
ECACC Cat# 91032111, RRID:CVCL_8V28 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 91032111 ECACC:91032111,
Wikidata:Q54828829
CVCL_8V28 2026-08-29 04:24:41 0

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