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Fisher, M. H.; Lense, M. D.; Dykens, E. M. – Journal of Intellectual Disability Research, 2016
Background: Williams syndrome (WS) is associated with a distinct cognitive-behavioural phenotype including mild to moderate intellectual disability, visual-spatial deficits, hypersociability, inattention and anxiety. Researchers typically characterise samples of individuals with WS by their intellectual functioning and adaptive behaviour. Because…
Descriptors: Genetic Disorders, Intellectual Disability, Cognitive Development, Adolescents

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