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Williams Syndrome (WS), aka Williams Beuren Syndrome, is a developmental disorder that we have known about for some forty years. The cause for WS was detected only recently: a micro deletion on chromosome 7, more specifically at the region of chromosome 7q11.23. The cognitive and behavioral profile in WS is characterized by a marked discrepancy between verbal and non-verbal skills combined with relatively spared linguistic skills. Recent research has shown considerable progress defining the areas of intactness in linguistic abilities. This volume builds on that research, giving an overview of the psycholinguistic research undertaken and opening up new perspectives and insights through new data and analyses. This book is of interest to researchers of applied cognitive science and to linguists more occupied with theoretical research.

Williams syndrome --- Language disorders in children --- Communicative disorders in children --- Beuren syndrome --- Contiguous gene syndrome --- Elfin facies syndrome --- Fanconi-Schlesinger syndrome --- Idiopathic hypercalcemia-supravalvular aortic stenosis syndrome --- Supravalvar aortic stenosis syndrome --- Williams-Barratt syndrome --- Williams-Beuren syndrome --- Williams contiguous gene syndrome --- Aortic valve stenosis in children --- Intellectual disability --- Syndromes in children --- Patients --- Language --- Neuropathology --- Sociolinguistics --- Psycholinguistics