Supernumerary marker 15 chromosome in a patient with Prader-Willi syndrome

Clin Genet. 2004 Mar;65(3):242-3. doi: 10.1111/j.0009-9163.2004.00203.x.
No abstract available

Publication types

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

MeSH terms

  • Adolescent
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 15*
  • Female
  • Humans
  • In Situ Hybridization, Fluorescence
  • Inheritance Patterns
  • Prader-Willi Syndrome / genetics*
  • Uniparental Disomy