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t(X;22)(p11;q13)

MedGen UID:
1763695
Concept ID:
C5420810
Cell or Molecular Dysfunction

Definition

A chromosomal translocation involving the BCOR gene at Xp11 and the ZC3H7B gene at 22q13. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVt(X;22)(p11;q13)

Recent clinical studies

Diagnosis

Hoang L, Chiang S, Lee CH
Pathology 2018 Feb;50(2):162-177. Epub 2017 Dec 22 doi: 10.1016/j.pathol.2017.11.086. PMID: 29275929

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