Smith-Magenis syndrome and tetralogy of Fallot

J Med Genet. 1999 Jun;36(6):501-2.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Chromosome Deletion
  • Chromosomes, Human, Pair 17 / genetics
  • Developmental Disabilities / genetics
  • Female
  • Humans
  • Infant
  • Male
  • Syndrome
  • Tetralogy of Fallot / genetics*