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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
DD3290
 
Resource Report
Resource Website
ECACC Cat# 98103009, RRID:CVCL_9M81 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 98103009 ECACC:98103009,
Wikidata:Q54830674
CVCL_9M81 2026-07-25 04:30:12 0
DD3284
 
Resource Report
Resource Website
ECACC Cat# 98102918, RRID:CVCL_9P22 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 98102918 ECACC:98102918,
Wikidata:Q54830668
CVCL_9P22 2026-07-25 04:30:12 0
DD3265
 
Resource Report
Resource Website
ECACC Cat# 98102706, RRID:CVCL_9M77 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 98102706 ECACC:98102706,
Wikidata:Q54830648
CVCL_9M77 2026-07-25 04:30:11 0
DD3312
 
Resource Report
Resource Website
ECACC Cat# 98111903, RRID:CVCL_9P30 Homo sapiens (Human) Karyotypic information: 46,XY,der(1)t(1;13)(q32.3;q32.3)mat (ECACC=98111903)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 98111903 ECACC:98111903,
Wikidata:Q54830686
CVCL_9P30 2026-07-25 04:30:13 0
DD3323
 
Resource Report
Resource Website
ECACC Cat# 98120706, RRID:CVCL_9P33 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 98120706 ECACC:98120706,
Wikidata:Q54830692
CVCL_9P33 2026-07-25 04:30:13 0
DD3280
 
Resource Report
Resource Website
ECACC Cat# 98102914, RRID:CVCL_9P18 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 98102914 ECACC:98102914,
Wikidata:Q54830664
CVCL_9P18 2026-07-25 04:30:12 0
DD3329
 
Resource Report
Resource Website
ECACC Cat# 98121012, RRID:CVCL_9P35 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Finite cell line Sex unspecified ECACC 98121012 ECACC:98121012,
Wikidata:Q54830700
CVCL_9P35 2026-07-25 04:30:13 0
DD3292
 
Resource Report
Resource Website
ECACC Cat# 98103011, RRID:CVCL_9M83 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 98103011 ECACC:98103011,
Wikidata:Q54830676
CVCL_9M83 2026-07-25 04:30:12 0
DD3310
 
Resource Report
Resource Website
ECACC Cat# 98111804, RRID:CVCL_9M88 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 98111804 ECACC:98111804,
Wikidata:Q54830685
CVCL_9M88 2026-07-25 04:30:13 0
DD3271
 
Resource Report
Resource Website
ECACC Cat# 98102905, RRID:CVCL_9P09 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 98102905 ECACC:98102905,
Wikidata:Q54830655
CVCL_9P09 2026-07-25 04:30:12 0
DD3306
 
Resource Report
Resource Website
ECACC Cat# 98111707, RRID:CVCL_9M87 Homo sapiens (Human) Karyotypic information: 46,XX,inv(17)(p?11;q?12) (ECACC=98111707)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 98111707 ECACC:98111707,
Wikidata:Q54830683
CVCL_9M87 2026-07-25 04:30:12 0
DD3276
 
Resource Report
Resource Website
ECACC Cat# 98102910, RRID:CVCL_9P14 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 98102910 ECACC:98102910,
Wikidata:Q54830660
CVCL_9P14 2026-07-25 04:30:12 0
DD3266
 
Resource Report
Resource Website
ECACC Cat# 98102817, RRID:CVCL_9M78 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 98102817 ECACC:98102817,
Wikidata:Q54830649
CVCL_9M78 2026-07-25 04:30:11 0
DD3282
 
Resource Report
Resource Website
ECACC Cat# 98102916, RRID:CVCL_9P20 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 98102916 ECACC:98102916,
Wikidata:Q54830666
CVCL_9P20 2026-07-25 04:30:12 0
DD3279
 
Resource Report
Resource Website
ECACC Cat# 98102913, RRID:CVCL_9P17 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 98102913 ECACC:98102913,
Wikidata:Q54830663
CVCL_9P17 2026-07-25 04:30:12 0
DD3291
 
Resource Report
Resource Website
ECACC Cat# 98103010, RRID:CVCL_9M82 Homo sapiens (Human) Type 1 diabetes mellitus Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 98103010 ECACC:98103010,
Wikidata:Q54830675
CVCL_9M82 2026-07-25 04:30:12 0
DD3333
 
Resource Report
Resource Website
ECACC Cat# 98121502, RRID:CVCL_9P37 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 98121502 ECACC:98121502,
Wikidata:Q54830702
CVCL_9P37 2026-07-25 04:30:13 0
DD3287
 
Resource Report
Resource Website
ECACC Cat# 98102921, RRID:CVCL_9P25 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 98102921 ECACC:98102921,
Wikidata:Q54830671
CVCL_9P25 2026-07-25 04:30:12 0
DD3281
 
Resource Report
Resource Website
ECACC Cat# 98102915, RRID:CVCL_9P19 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 98102915 ECACC:98102915,
Wikidata:Q54830665
CVCL_9P19 2026-07-25 04:30:12 0
DD3303
 
Resource Report
Resource Website
ECACC Cat# 98111204, RRID:CVCL_9P28 Homo sapiens (Human) Fragile X syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 98111204 ECACC:98111204,
Wikidata:Q54830682
CVCL_9P28 2026-07-25 04:30:13 0

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