Klinefelter and trisomy X syndromes in patients with Prader-Willi syndrome and uniparental maternal disomy of chromosome 15--a coincidence?

Am J Med Genet. 1997 Oct 3;72(1):111-4.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Child
  • Chromosomes, Human, Pair 15 / genetics*
  • Female
  • Humans
  • Klinefelter Syndrome / genetics*
  • Male
  • Prader-Willi Syndrome / genetics*
  • Trisomy / genetics*
  • X Chromosome*