Common and specific impairments in attention functioning in girls with chromosome 22q11.2 deletion, fragile X or Turner syndromes

Bibliographic Details
Main Authors: Quintero, Andrea I, Beaton, Elliott A, Harvey, Danielle J, Ross, Judith L, Simon, Tony J
Format: Online
Language:English
Published: BioMed Central 2014
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3995552/