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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
DD1614
 
Resource Report
Resource Website
ECACC Cat# 93112613, RRID:CVCL_9G73 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 93112613 ECACC:93112613,
Wikidata:Q54829884
CVCL_9G73 2026-07-25 04:29:49 0
DD1551
 
Resource Report
Resource Website
ECACC Cat# 93102213, RRID:CVCL_AQ74 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 93102213 ECACC:93102213,
Wikidata:Q54829842
CVCL_AQ74 2026-07-25 04:29:48 0
DD1613
 
Resource Report
Resource Website
ECACC Cat# 93112612, RRID:CVCL_9G72 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 93112612 ECACC:93112612,
Wikidata:Q54829883
CVCL_9G72 2026-07-25 04:29:49 0
DD1622
 
Resource Report
Resource Website
ECACC Cat# 93112929, RRID:CVCL_9G77 Homo sapiens (Human) Holoprosencephaly Karyotypic information: 46,XY,del(2)(pter->?p22.1::?p21->qter); de novo (ECACC=93112929)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 93112929 ECACC:93112929,
Wikidata:Q54829889
CVCL_9G77 2026-07-25 04:29:49 0
DD1550
 
Resource Report
Resource Website
ECACC Cat# 93102212, RRID:CVCL_9G40 Homo sapiens (Human) Karyotypic information: 46,X,der(X),t(X;10)(Xpter->q26;q24->10qter)mat (ECACC=93102212)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 93102212 ECACC:93102212,
Wikidata:Q54829841
CVCL_9G40 2026-07-25 04:29:48 0
DD1571
 
Resource Report
Resource Website
ECACC Cat# 93110301, RRID:CVCL_9G49 Homo sapiens (Human) Karyotypic information: 47,XX,+dic(15); de novo (ECACC=93110301)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 93110301 ECACC:93110301,
Wikidata:Q54829851
CVCL_9G49 2026-07-25 04:29:48 0
DD1619
 
Resource Report
Resource Website
ECACC Cat# 93112926, RRID:CVCL_9G75 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 93112926 ECACC:93112926,
Wikidata:Q54829887
CVCL_9G75 2026-07-25 04:29:49 0
DD1561
 
Resource Report
Resource Website
ECACC Cat# 93102803, RRID:CVCL_9G44 Homo sapiens (Human) Developmental delay Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 93102803 ECACC:93102803,
Wikidata:Q54829846
CVCL_9G44 2026-07-25 04:29:48 0
DD1583
 
Resource Report
Resource Website
ECACC Cat# 93110418, RRID:CVCL_AQ75 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 93110418 ECACC:93110418,
Wikidata:Q54829862
CVCL_AQ75 2026-07-25 04:29:48 0
DD1617
 
Resource Report
Resource Website
ECACC Cat# 93112924, RRID:CVCL_AQ82 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 93112924 ECACC:93112924,
Wikidata:Q54829885
CVCL_AQ82 2026-07-25 04:29:49 0
DD1710
 
Resource Report
Resource Website
ECACC Cat# 94011411, RRID:CVCL_9H14 Homo sapiens (Human) Hydrops fetalis Karyotypic information: 47,XX,+13 (ECACC=94011411)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 94011411 ECACC:94011411,
Wikidata:Q54829930
CVCL_9H14 2026-07-25 04:29:50 0
DD1733
 
Resource Report
Resource Website
ECACC Cat# 94012812, RRID:CVCL_9H28 Homo sapiens (Human) Karyotypic information: 46,XX,t(10;16;20); de novo (ECACC=94012812)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 94012812 ECACC:94012812,
Wikidata:Q54829944
CVCL_9H28 2026-07-25 04:29:51 0
DD1662
 
Resource Report
Resource Website
ECACC Cat# 93121701, RRID:CVCL_9G96 Homo sapiens (Human) Trisomy 18 Karyotypic information: 47,XY,+18 (ECACC=93121701)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 93121701 ECACC:93121701,
Wikidata:Q54829909
CVCL_9G96 2026-07-25 04:29:50 0
DD1661
 
Resource Report
Resource Website
ECACC Cat# 93121505, RRID:CVCL_9G95 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 93121505 ECACC:93121505,
Wikidata:Q54829908
CVCL_9G95 2026-07-25 04:29:50 0
DD1658
 
Resource Report
Resource Website
ECACC Cat# 93121412, RRID:CVCL_9G93 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 93121412 ECACC:93121412,
Wikidata:Q54829906
CVCL_9G93 2026-07-25 04:29:50 0
DD1699
 
Resource Report
Resource Website
ECACC Cat# 94010713, RRID:CVCL_9H08 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 94010713 ECACC:94010713,
Wikidata:Q54829924
CVCL_9H08 2026-07-25 04:29:50 0
DD1688
 
Resource Report
Resource Website
ECACC Cat# 93122217, RRID:CVCL_9H03 Homo sapiens (Human) Trisomy 18 Karyotypic information: 47,XX,+18 (ECACC=93122217)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 93122217 ECACC:93122217,
Wikidata:Q54829917
CVCL_9H03 2026-07-25 04:29:50 0
DD1709
 
Resource Report
Resource Website
ECACC Cat# 94011410, RRID:CVCL_9H13 Homo sapiens (Human) Congenital cystic hygroma Karyotypic information: 69,XXX (ECACC=94011410)., Part of: ECACC chromosomal abnormality collection. Finite cell line Sex ambiguous ECACC 94011410 ECACC:94011410,
Wikidata:Q54829929
CVCL_9H13 2026-07-25 04:29:50 0
DD1642
 
Resource Report
Resource Website
ECACC Cat# 93120317, RRID:CVCL_9G84 Homo sapiens (Human) Trisomy 18 Karyotypic information: 47,XY,+18 (ECACC=93120317)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 93120317 ECACC:93120317,
Wikidata:Q54829897
CVCL_9G84 2026-07-25 04:29:49 0
DD1640
 
Resource Report
Resource Website
ECACC Cat# 93120315, RRID:CVCL_9G82 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 93120315 ECACC:93120315,
Wikidata:Q54829895
CVCL_9G82 2026-07-25 04:29:49 0

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