Article

Williams Syndrome-Specific Neuroarchitectural Profile and Its Associations with Cognitive Features

2016-06-26

Abstract excerpt

Williams Syndrome (WS), a rare genetic disorders caused by hemizyous deletion of ~26 genes on the chromosome 7, has unique cognitive features and neuroanatomic abnormalities. Limited in statistical power due to its rareness had led to inconsistent in many direct comparisons using structural magnetic resonance imaging (MRI), and their associations with cognitive features of WS are not clear. Here, we used a novel a...

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Literature Corpus work: 267c7314-b94d-5400-ad13-287d32279f95
DOI: 10.1101/060764

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