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t(4;14)(p16;q32)

MedGen UID:
925470
Concept ID:
C4287938
Cell or Molecular Dysfunction

Definition

A cytogenetic abnormality that refers to the translocation of the short arm (p16) of chromosome 4 and the long arm (q32) of chromosome 14. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVt(4;14)(p16;q32)

Professional guidelines

PubMed

de Brito LR, Batey MA, Zhao Y, Squires MS, Maitland H, Leung HY, Hall AG, Jackson G, Newell DR, Irving JA
Leuk Res 2011 Sep;35(9):1233-40. Epub 2011 Feb 11 doi: 10.1016/j.leukres.2011.01.011. PMID: 21316102
Fonseca R, Bergsagel PL, Drach J, Shaughnessy J, Gutierrez N, Stewart AK, Morgan G, Van Ness B, Chesi M, Minvielle S, Neri A, Barlogie B, Kuehl WM, Liebisch P, Davies F, Chen-Kiang S, Durie BG, Carrasco R, Sezer O, Reiman T, Pilarski L, Avet-Loiseau H; International Myeloma Working Group
Leukemia 2009 Dec;23(12):2210-21. Epub 2009 Oct 1 doi: 10.1038/leu.2009.174. PMID: 19798094Free PMC Article

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