Non-chromosome 15 marker chromosome in a Prader-Willi syndrome patient with uniparental disomy

Pediatr Int. 2006 Feb;48(1):97-9. doi: 10.1111/j.1442-200X.2006.02163.x.
No abstract available

Publication types

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

MeSH terms

  • Child
  • Chromosome Aberrations*
  • Female
  • Humans
  • Karyotyping
  • Male
  • Prader-Willi Syndrome / genetics*
  • Uniparental Disomy / genetics*