Characterization of two marker chromosomes in a patient with acute nonlymphocytic leukemia by two-color fluorescence in situ hybridization

Cancer Genet Cytogenet. 1993 Oct 15;70(2):99-102. doi: 10.1016/0165-4608(93)90175-l.

Abstract

A patient with acute nonlymphocytic leukemia (ANLL), M5b according to French-American-British (FAB) classification, showed monosomy 16, an extra 1p-, and a 21q+. These derivative chromosomes could not be defined by GTG-banding. For better characterization, we performed two-color fluorescence in situ hybridization (FISH) experiments applying DNA libraries from sorted human chromosomes, chromosome-specific repetitive probes, and a band-specific YAC-clone. With these FISH studies the karyotype could be characterized as 46,XY, +der(1)t(1;21)(p11;?), -16,der(21)t(16;21) (p11.1;q22).

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Chromosome Aberrations*
  • Chromosome Banding
  • Chromosomes, Artificial, Yeast
  • Chromosomes, Human, Pair 1*
  • Chromosomes, Human, Pair 16*
  • Chromosomes, Human, Pair 21*
  • DNA Probes
  • Gene Library
  • Genetic Markers
  • Humans
  • In Situ Hybridization, Fluorescence
  • Karyotyping
  • Leukemia, Myeloid, Acute / genetics*
  • Male
  • Monosomy
  • Translocation, Genetic

Substances

  • DNA Probes
  • Genetic Markers