Angelman syndrome caused by an identical familial 1,487-kb deletion

Am J Med Genet A. 2007 Jan 1;143A(1):98-101. doi: 10.1002/ajmg.a.31550.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Angelman Syndrome / diagnosis
  • Angelman Syndrome / genetics*
  • Base Sequence
  • Child, Preschool
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 15 / genetics*
  • DNA Mutational Analysis
  • Female
  • Humans
  • In Situ Hybridization, Fluorescence
  • Male
  • Pedigree
  • Phenotype