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t(1;22)(q23;q12)

MedGen UID:
1739959
Concept ID:
C5420795
Cell or Molecular Dysfunction

Definition

A chromosomal translocation involving the PBX1 gene at 1q23 and the EWSR1 gene at 22q12. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVt(1;22)(q23;q12)

Supplemental Content

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