Molecular characterization of a (1;10)(p22;q21) constitutional translocation from a patient with neuroblastoma

R. Scott Mead, John K. Cowell

Research output: Contribution to journalArticle

20 Scopus citations

Abstract

A constitutional t(1;10)(p22;q21) from a patient with stage IVS neuroblastoma has been isolated in somatic cell hybrids and the position of the breakpoints analyzed. On chromosome 1 the breakpoint lies in a 4-Mbp region flanked by minisatellite marker D1S234 and by D1S188, which lies in the region of F3. The chromosome 10 breakpoint lies between RBP3 and NAKNR below the MEN2 locus. Because, in patients with genetic disease, constitutional translocations frequently interrupt genes which are related to the clinical phenotype this rearrangement has identified two regions which potentially contain genes related to the development of neuroblastoma.

Original languageEnglish (US)
Pages (from-to)151-157
Number of pages7
JournalCancer Genetics and Cytogenetics
Volume81
Issue number2
DOIs
StatePublished - Jun 1995

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Cancer Research

Fingerprint Dive into the research topics of 'Molecular characterization of a (1;10)(p22;q21) constitutional translocation from a patient with neuroblastoma'. Together they form a unique fingerprint.

  • Cite this