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Direct linkHowlin, Patricia; Elison, Sarah; Udwin, Orlee; Stinton, Christopher – Journal of Applied Research in Intellectual Disabilities, 2010
Background: Little is known about trajectories of cognitive functioning as individuals with Williams syndrome (WS) move though adulthood. Method: The present study investigated cognitive, linguistic and adaptive functioning in adults with WS aged 19-55 years, using both cross-sectional and longitudinal approaches. Results: Data from the…
Descriptors: Comprehension, Mental Retardation, Linguistics, Intelligence Quotient
