Middle and inner ear malformations in velocardiofacial syndrome

Am J Med Genet A. 2004 Dec 1;131(2):225-6. doi: 10.1002/ajmg.a.30326.
No abstract available

Publication types

  • Case Reports
  • Comment
  • Letter

MeSH terms

  • Child
  • Chromosome Deletion
  • Chromosomes, Human, Pair 2*
  • Craniofacial Abnormalities*
  • Ear, Inner / abnormalities*
  • Ear, Middle / abnormalities*
  • Female
  • Hearing Loss / genetics
  • Heart Defects, Congenital*
  • Humans
  • Syndrome