Inter- and intrachromosomal rearrangements are both involved in the origin of 15q11-q13 deletions in Prader-Willi syndrome

Am J Hum Genet. 1997 Jul;61(1):228-31. doi: 10.1086/513907.
No abstract available

Publication types

  • Letter

MeSH terms

  • Chromosomes, Human, Pair 15*
  • Female
  • Gene Deletion*
  • Gene Rearrangement*
  • Humans
  • Male
  • Prader-Willi Syndrome / genetics*