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....

por Quintela, Ines, Fernandez-Prieto, Montse, Gomez-Guerrero, Lorena, Resches, Mariela, Eiris, Jesus, Barros, Francisco, Carracedo, Angel
Publicado 2015