Research on behavioral phenotypes: velocardiofacial syndrome (deletion 22q11.2)

Dev Med Child Neurol. 2000 Jun;42(6):422-7. doi: 10.1017/s0012162200000785.
No abstract available

Publication types

  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Brain / abnormalities
  • Child
  • Child, Preschool
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 22 / genetics*
  • Humans
  • Memory Disorders / genetics
  • Mental Disorders / genetics*
  • Neuropsychological Tests
  • Phenotype
  • Syndrome
  • Velopharyngeal Insufficiency / genetics*