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t(5;17)(q35;q21)

MedGen UID:
884402
Concept ID:
C4053814
Cell or Molecular Dysfunction

Definition

A chromosomal abnormality consisting of the translocation of 5q32 with 17q21. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVt(5;17)(q35;q21)

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