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

First Author: Pagnamenta AT
Attributed to:  The Autism Genome Project funded by MRC


No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1136/jmg.2010.079426

PubMed Identifier: 20972252

Publication URI: http://europepmc.org/abstract/MED/20972252

Type: Journal Article/Review

Volume: 48

Parent Publication: Journal of medical genetics

Issue: 1

ISSN: 0022-2593