Genomic imprinting in an Angelman and Prader-Willi translocation family

Lancet. 1991 Sep 7;338(8767):638-9. doi: 10.1016/0140-6736(91)90652-6.
No abstract available

Publication types

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

MeSH terms

  • Child
  • Chromosome Aberrations / genetics*
  • Chromosome Deletion
  • Chromosome Disorders
  • Chromosomes, Human, Pair 15*
  • Female
  • Humans
  • Male
  • Pedigree
  • Phenotype
  • Prader-Willi Syndrome / genetics*
  • Translocation, Genetic / genetics*