A supernumerary marker chromosome 15 tetrasomic for the Prader-Willi/Angelman syndrome critical region in a patient with a severe phenotype

J Med Genet. 2003 Jul;40(7):e84. doi: 10.1136/jmg.40.7.e84.
No abstract available

Publication types

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

MeSH terms

  • Aneuploidy*
  • Angelman Syndrome / genetics*
  • Child
  • Chromosome Inversion
  • Chromosomes, Human, Pair 15 / genetics*
  • Humans
  • In Situ Hybridization, Fluorescence
  • Male
  • Microsatellite Repeats
  • Phenotype
  • Prader-Willi Syndrome / genetics*