Impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome

Impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome

<p>Abstract</p> <p>Background</p> <p>Chromosome 22q11.2 Deletion Syndrome (22q11.2DS) occurs in approximately 1:4,000 live births with a complex and variable presentation that includes medical, socioemotional and psychological symptoms with intellectual impairment. Cogn...

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Bibliographic Details
Main Authors: Cabaral Margarita H, Beaton Elliott A, Stoddard Joel, Simon Tony J
Format: Article
Language:English
Published: BMC 2012-04-01
Series:Journal of Neurodevelopmental Disorders
Subjects:
Attention
Children
Chromosome 22q11.2 deletion syndrome (22q11.2DS)
DiGeorge Syndrome
Multiple object tracking
Spatiotemporal attention
Velocardiofacial syndrome (VCFS)
Online Access:http://www.jneurodevdisorders.com/content/4/1/6

Internet

http://www.jneurodevdisorders.com/content/4/1/6

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