Genotype and phenotype in Angelman syndrome caused by paternal UPD 15

Am J Med Genet. 1997 Jun 13;70(3):328-9. doi: 10.1002/(sici)1096-8628(19970613)70:3<328::aid-ajmg21>3.0.co;2-m.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Angelman Syndrome / genetics*
  • Child
  • Chromosomes, Human, Pair 15*
  • Fathers*
  • Genomic Imprinting*
  • Genotype
  • Humans
  • In Situ Hybridization, Fluorescence
  • Karyotyping
  • Phenotype