Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial duplication of Yq (Yq11.2-->qter) and partial monosomy 5p (5p15.3-->pter)

Prenat Diagn. 2005 Aug;25(8):723-5. doi: 10.1002/pd.1223.
No abstract available

Publication types

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

MeSH terms

  • Adult
  • Chromosome Aberrations
  • Chromosomes, Human, Pair 5 / genetics*
  • Chromosomes, Human, Y / genetics*
  • Cri-du-Chat Syndrome / genetics*
  • Female
  • Fetal Growth Retardation / diagnostic imaging
  • Fetal Growth Retardation / genetics
  • Flow Cytometry
  • Fluorescence
  • Gene Duplication
  • Humans
  • In Situ Hybridization, Fluorescence
  • Infant, Newborn
  • Karyotyping
  • Male
  • Monosomy / genetics*
  • Pregnancy
  • Ultrasonography, Prenatal