Publication:

Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability (2011)

Author(s): Pagnamenta AT, Khan H, Walker S, Gerrelli D, Wing K, Bonaglia MC, Giorda R, Berney T, Mani E, Molteni M, Pinto D, Le Couteur A, Hallmayer J, Sutcliffe JS, Szatmari P, Paterson AD, Scherer SW, Vieland VJ, Monaco AP

      • Date: 23-10-2010
      • Journal: Journal of Medical Genetics
      • Volume: 48
      • Issue: 1
      • Pages: 48-54
      • Publisher: BMJ Group
      • Publication type: Article
      • Bibliographic status: Published

      Keywords: COPY NUMBER VARIATION SPECTRUM DISORDERS GENOME LOCI ASSOCIATION MUTATIONS SHANK3 PHENOTYPES GENES

      Staff

      Professor Ann Le Couteur
      Professor of Child & Adolescent Psychiatry