Identification of iso(18p) marker chromosome by fluorescence in situ hybridization with single-copy DNA probe

Jpn J Hum Genet. 1995 Jun;40(2):185-8. doi: 10.1007/BF01883575.

Abstract

The patient displayed the clinical features consistent with tetrasomy (18p) syndrome, who had an extra small metacentric iso(18p) chromosome in otherwise normal karyotype. Identification of the marker chromosome used the chromosome 18 band-specific fluorescence in situ hybridization strategy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Chromosome Aberrations*
  • Chromosomes, Human, Pair 18*
  • DNA Probes
  • Genetic Markers
  • Humans
  • In Situ Hybridization, Fluorescence
  • Male
  • Microcephaly / genetics

Substances

  • DNA Probes
  • Genetic Markers