Further example of a patient with Prader-Willi and Klinefelter syndromes of different parental origins

Am J Med Genet. 1998 Nov 16;80(3):286-7.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Child
  • Chromosomes, Human, Pair 15*
  • Genomic Imprinting*
  • Humans
  • Klinefelter Syndrome / complications
  • Klinefelter Syndrome / genetics*
  • Prader-Willi Syndrome / complications
  • Prader-Willi Syndrome / genetics*
  • X Chromosome*