Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability
published in: Journal of Medical Genetics
date of publication: 2011-01
language: English
main subject: disability, autism, learning disability
Cites articles 34
- 2009-04-01
Date
Title
Article - wd:Q28296551