ArticleAmerican journal of human genetics2015
Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling.
Lot Snijders Blok et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.
177 papers cite itlatest 60 shown
this paperpooled ittrialcites it