Genetic basis of Prader-Willi syndrome in Korea: less uniparental disomy than has been recognized?

Clin Genet. 2004 Oct;66(4):368-72. doi: 10.1111/j.1399-0004.2004.00323.x.
No abstract available

Publication types

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

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • Chromosome Deletion
  • Chromosomes, Human, Pair 15*
  • Female
  • Genomic Imprinting*
  • Humans
  • Infant
  • Korea
  • Male
  • Maternal Age
  • Mothers
  • Prader-Willi Syndrome / diagnosis
  • Prader-Willi Syndrome / genetics*
  • Uniparental Disomy*