Prader-Willi or Angelman syndrome in familial 15q11----q13 deletion of maternal origin?

Hum Genet. 1992 Jan;88(3):361-2. doi: 10.1007/BF00197279.
No abstract available

Publication types

  • Letter

MeSH terms

  • Chromosome Deletion*
  • Chromosomes, Human, Pair 15*
  • Epilepsy / genetics*
  • Female
  • Humans
  • Intellectual Disability / genetics*
  • Male
  • Prader-Willi Syndrome / genetics*
  • Pregnancy
  • Syndrome