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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
DD3129
 
Resource Report
Resource Website
ECACC Cat# 98050115, RRID:CVCL_9M40 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 98050115 ECACC:98050115,
Wikidata:Q54830582
CVCL_9M40 2026-08-15 04:27:00 0
DD3098
 
Resource Report
Resource Website
RRID:CVCL_9M28 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Finite cell line Sex unspecified ECACC:98040204,
Wikidata:Q54830563
CVCL_9M28 2026-08-15 04:26:59 0
DD3073
 
Resource Report
Resource Website
RRID:CVCL_9M09 Homo sapiens (Human) Karyotypic information: 46,XY,t(1;8)(p32;q13); de novo (ECACC=98031003)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC:98031003,
Wikidata:Q54830544
CVCL_9M09 2026-08-15 04:26:59 0
DD3090
 
Resource Report
Resource Website
RRID:CVCL_9M23 Homo sapiens (Human) Karyotypic information: 47,XXY,t(3;4)(q26.32;q31.1)mat (ECACC=98032405)., Part of: ECACC chromosomal abnormality collection. Finite cell line Sex ambiguous ECACC:98032405,
Wikidata:Q54830558
CVCL_9M23 2026-08-15 04:27:00 0
DD3126
 
Resource Report
Resource Website
ECACC Cat# 980427186, RRID:CVCL_9M37 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 980427186 ECACC:980427186,
Wikidata:Q54830579
CVCL_9M37 2026-08-15 04:27:00 0
DD3131
 
Resource Report
Resource Website
ECACC Cat# 98050117, RRID:CVCL_9M42 Homo sapiens (Human) Type 1 diabetes mellitus Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 98050117 ECACC:98050117,
Wikidata:Q54830584
CVCL_9M42 2026-08-15 04:27:00 0
DD3121
 
Resource Report
Resource Website
RRID:CVCL_9N78 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC:98042303,
Wikidata:Q54830578
CVCL_9N78 2026-08-15 04:27:00 0
DD3086
 
Resource Report
Resource Website
ECACC Cat# 98032003, RRID:CVCL_9M19 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 98032003 ECACC:98032003,
Wikidata:Q54830554
CVCL_9M19 2026-08-15 04:26:59 0
DD3106
 
Resource Report
Resource Website
ECACC Cat# 98041712, RRID:CVCL_9M33 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 98041712 ECACC:98041712,
Wikidata:Q54830570
CVCL_9M33 2026-08-15 04:27:00 0
DD3095
 
Resource Report
Resource Website
ECACC Cat# 98040201, RRID:CVCL_9M25 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 98040201 ECACC:98040201,
Wikidata:Q54830560
CVCL_9M25 2026-08-15 04:26:59 0
DD3115
 
Resource Report
Resource Website
ECACC Cat# 98042011, RRID:CVCL_9M35 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 98042011 ECACC:98042011,
Wikidata:Q54830574
CVCL_9M35 2026-08-15 04:27:00 0
DD3113
 
Resource Report
Resource Website
RRID:CVCL_9M34 Homo sapiens (Human) Karyotypic information: 46,XX,del(22)(q13) (ECACC=98042009)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:98042009,
Wikidata:Q54830573
CVCL_9M34 2026-08-15 04:27:00 0
DD3099
 
Resource Report
Resource Website
ECACC Cat# 98040205, RRID:CVCL_9M29 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 98040205 ECACC:98040205,
Wikidata:Q54830564
CVCL_9M29 2026-08-15 04:26:59 0
DD3082
 
Resource Report
Resource Website
RRID:CVCL_9M15 Homo sapiens (Human) Congenital eyelid ptosis Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:98031908,
Wikidata:Q54830550
CVCL_9M15 2026-08-15 04:26:59 0
DD3100
 
Resource Report
Resource Website
RRID:CVCL_9M30 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC:98040801,
Wikidata:Q54830565
CVCL_9M30 2026-08-15 04:27:00 0
DD3076
 
Resource Report
Resource Website
RRID:CVCL_9M11 Homo sapiens (Human) Goldenhar syndrome Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC:98031011,
Wikidata:Q54830546
CVCL_9M11 2026-08-15 04:27:00 0
DD3121
 
Resource Report
Resource Website
ECACC Cat# 98042303, RRID:CVCL_9N78 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 98042303 ECACC:98042303,
Wikidata:Q54830578
CVCL_9N78 2026-08-15 04:27:00 0
DD3072
 
Resource Report
Resource Website
RRID:CVCL_9M08 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:98031002,
Wikidata:Q54830543
CVCL_9M08 2026-08-15 04:26:59 0
DD3078
 
Resource Report
Resource Website
ECACC Cat# 98031013, RRID:CVCL_9M13 Homo sapiens (Human) Nevus of Ito Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 98031013 ECACC:98031013,
Wikidata:Q54830548
CVCL_9M13 2026-08-15 04:26:59 0
DD3083
 
Resource Report
Resource Website
ECACC Cat# 98031909, RRID:CVCL_9M16 Homo sapiens (Human) Congenital eyelid ptosis Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 98031909 ECACC:98031909,
Wikidata:Q54830551
CVCL_9M16 2026-08-15 04:26:59 0

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