Social Cognition in Williams Syndrome: Genotype/Phenotype Insights from Partial Deletion Patients

Abstract

Identifying genotype/phenotype relations in human social cognition has been enhanced by the study of Williams syndrome (WS). Indeed, individuals with WS present with a particularly strong social drive, and researchers have sought to link deleted genes in the WS critical region (WSCR) of chromosome 7q11.23 to this unusual social profile. In this paper, we… (More)
DOI: 10.3389/fpsyg.2012.00168

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