Exclusion of 22q11 deletion in Noonan syndrome with tetralogy of Fallot

Am J Med Genet. 1996 Apr 24;62(4):413-4. doi: 10.1002/ajmg.1320620404.
No abstract available

Publication types

  • Case Reports
  • Comment
  • Letter

MeSH terms

  • Child
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 22*
  • Female
  • Humans
  • Infant
  • Male
  • Noonan Syndrome / complications
  • Noonan Syndrome / genetics*
  • Tetralogy of Fallot / complications
  • Tetralogy of Fallot / genetics*