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

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
J Med Genet. 2011 48 (1): 48-54

PMID: 20972252 · PMCID: PMC3003876 · DOI:10.1136/jmg.2010.079426

MeSH Terms (23)

Adolescent Autistic Disorder Base Sequence Cadherins Child Chromosome Deletion Chromosomes, Human, Pair 16 DNA Copy Number Variations DNA Mutational Analysis Family Female Gene Expression Regulation Genetic Linkage Genetic Predisposition to Disease Genome, Human Humans Intelligence Tests Internet Learning Disabilities Male Molecular Sequence Data Pedigree Young Adult

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