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

Author： Woodcock Kate   Oliver Chris   Humphreys Glyn  

Publisher： Routledge Ltd

ISSN： 1464-0627

Source： Cognitive Neuropsychology, Vol.26, Iss.2, 2009-02, pp. : 172-194

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Deficits in Social Attribution Ability in Prader–Willi Syndrome

By Koenig Kathleen   Klin Ami   Schultz Robert  

Journal of Autism and Developmental Disorders, Vol. 34, Iss. 5, 2004-10 ,pp. : 573-582

Springer Publishing Company

Access to resources Recommend Favorite

Angelman syndrome: Genetic mechanisms and relationship to Prader-Willi syndrome 1

By Smith Arabella  

Journal of Intellectual & Developmental Disability, Vol. 19, Iss. 4, 1994-01 ,pp. : 259-267

Informa Healthcare

Access to resources Recommend Favorite

NEUROPSYCHOLOGICAL CHARACTERISTICS OF CHILDREN WITH THE 22Q11 DELETION SYNDROME: A DESCRIPTIVE ANALYSIS

By Sobin Christina   Kiley-Brabeck Karen   Daniels Sarah   Khuri Jananne   Taylor Lisa   Blundell Maude   Anyane-Yeboa Kwame   Karayiorgou Maria  

Child Neuropsychology (Neuropsychology, Development and Cognition: Section C), Vol. 11, Iss. 1, 2005-02 ,pp. : 39-53

Routledge Ltd

Access to resources Recommend Favorite

Catatonia in an Adolescent with Prader–Willi Syndrome

By Dhossche D.M.  

Annals of Clinical Psychiatry (after Jan 1, 2004), Vol. 09, Iss. 4, 1997-12 ,pp. : 247-253

Springer Publishing Company

Access to resources Recommend Favorite

Prader-Willi syndrome and hyperphagia: an update

By Stanley K.  

Advances in Mental Health and Intellectual Disabilities, Vol. 8, Iss. 5, 2014-08 ,pp. : 321-330

Emerald Group Publishing Ltd

Access to resources Recommend Favorite