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

标题
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability
作者
关键词
-
出版物
JOURNAL OF MEDICAL GENETICS
Volume 48, Issue 1, Pages 48-54
出版商
BMJ
发表日期
2010-10-24
DOI
10.1136/jmg.2010.079426

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