Narrowing the critical deletion region for autism spectrum disorders on 16p11.2

Am J Med Genet B Neuropsychiatr Genet. 2011 Mar;156(2):243-5. doi: 10.1002/ajmg.b.31163. Epub 2011 Jan 11.
No abstract available

Publication types

  • Case Reports
  • Comparative Study
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Child
  • Child Development Disorders, Pervasive / genetics*
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 16*
  • Comparative Genomic Hybridization
  • Female
  • Genetic Predisposition to Disease
  • Heterozygote
  • Humans
  • Male
  • Nuclear Family
  • Pedigree
  • Risk Factors