A 6q14.1-q15 microdeletion in a male patient with severe autistic disorder, lack of oral language, and dysmorphic features with concomitant presence of a maternally inherited Xp22.31 copy number gain

Identifiers
Identifiers
Date issued
2015Journal title
Clinical Case Reports
Type of content
Artigo
Except where otherwise noted, this item's license is described as Attribution-NonCommercial 4.0 Internacional
