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Tags: Harvey D J

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

BACKGROUND: Chromosome 22q11.2 deletion syndrome (22q11.2DS), fragile X syndrome (FXS), and Turner syndrome (TS) are complex and variable developmental syndromes caused by different genetic abnormalities; yet, they share similar cognitive impairments…

Tags: 2014, 22q11.2 Deletion Syndrome, alertness, Attention, attention control, Beaton E A, characteristics, Harvey D J, Journal of Neurodevelopmental Disorders, Quintero A I, Ross J L, Simon T J, Trajectory

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