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t(1;13)(p36;q14)

MedGen UID:
881712
Concept ID:
C4053816
Cell or Molecular Dysfunction

Definition

A chromosomal translocation involving the PAX7 gene on chromosome 1p36 and the FOXO1 gene on chromosome 13q14. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVt(1;13)(p36;q14)

Professional guidelines

PubMed

Koscielniak E, Morgan M, Treuner J
Paediatr Drugs 2002;4(1):21-8. doi: 10.2165/00128072-200204010-00003. PMID: 11817983
Dockhorn-Dworniczak B, Schäfer KL, Blasius S, Christiansen H, Koscielniak E, Ritter J, Winkelmann W, Jürgens H, Böcker W
Klin Padiatr 1997 Jul-Aug;209(4):156-64. doi: 10.1055/s-2008-1043964. PMID: 9293447

Supplemental Content

Table of contents

    Practice guidelines

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