Prader-Willi syndrome due to 15q11-q13 deletion in a girl with an inherited (13;14) Robertsonian translocation

Am J Med Genet. 2002 Dec 1;113(3):307-8. doi: 10.1002/ajmg.10799.
No abstract available

Publication types

  • Letter

MeSH terms

  • Child, Preschool
  • Chromosomes, Human, Pair 15*
  • DNA Methylation
  • Female
  • Humans
  • In Situ Hybridization, Fluorescence
  • Infant
  • Infant, Newborn
  • Prader-Willi Syndrome / genetics*
  • Sequence Deletion*
  • Translocation, Genetic*