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Task-switching deficits and repetitive behaviour in genetic neurodevelopmental disorders: data from children with Prader-Willi syndrome chromosome 15 q11-q13 deletion and boys with Fragile X syndrome
scientific article
Author/s
author: Christopher Oliver, Kate A. Woodcock, Glyn W. Humphreys
Work details
Publication date
February 14, 2009
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Language
English
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