Cayler cardiofacial syndrome and del 22q11: part of the CATCH22 phenotype

Am J Med Genet. 1994 Nov 15;53(3):303-4. doi: 10.1002/ajmg.1320530320.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Child, Preschool
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 22*
  • Face / abnormalities
  • Facial Muscles / abnormalities*
  • Facial Paralysis / etiology
  • Heart Defects, Congenital / genetics
  • Humans
  • Infant
  • Syndrome