High resolution chromosome analysis and fluorescence in situ hybridization in patients referred for Prader-Willi or Angelman syndrome

Am J Med Genet. 1995 May 8;56(4):420-2. doi: 10.1002/ajmg.1320560414.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Adolescent
  • Adult
  • Angelman Syndrome / diagnosis*
  • Angelman Syndrome / genetics
  • Child
  • Child, Preschool
  • Chromosome Mapping*
  • Female
  • Humans
  • In Situ Hybridization, Fluorescence
  • Male
  • Prader-Willi Syndrome / diagnosis*
  • Prader-Willi Syndrome / genetics
  • Referral and Consultation