Cardio-facio-cutaneous syndrome phenotype and del(12q)

Am J Med Genet A. 2003 Feb 1;116A(4):411-2. doi: 10.1002/ajmg.a.10013.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Chromosomes, Human, Pair 12*
  • Facies
  • Heart Defects, Congenital / genetics
  • Humans
  • Noonan Syndrome / diagnosis
  • Noonan Syndrome / genetics
  • Phenotype*
  • Skin Abnormalities / genetics
  • Syndrome