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Prader–Willi syndrome

from Part IX - Developmental pathology

Published online by Cambridge University Press:  26 October 2017

Brian Hopkins
Affiliation:
Lancaster University
Elena Geangu
Affiliation:
Lancaster University
Sally Linkenauger
Affiliation:
Lancaster University
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Publisher: Cambridge University Press
Print publication year: 2017

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References

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Schulze, A., Mogensen, H., Hamborg-Petersen, B., Graem, N., Ostergaard, J.R., & Brøndum-Nielsen, K. (2001). Fertility in Prader–Willi syndrome: A case report with Angelman syndrome in the offspring. Acta Paediatrica, 90, 455459.CrossRefGoogle ScholarPubMed
Soni, S., Whittington, J., Holland, A.J., Webb, T., Maina, E.N., Boer, H., & Clarke, D. (2008). The phenomenology and diagnosis of psychiatric illness in people with Prader–Willi syndrome. Psychological Medicine, 38, 15051514.CrossRefGoogle ScholarPubMed
Stauder, J.E., Boer, H., Gerits, R.H., Tummers, A., Whittington, J., & Curfs, L.M. (2005). Differences in behavioural phenotype between parental deletion and maternal uniparental disomy in Prader–Willi syndrome: An ERP study. Clinical Neurophysiology, 116, 14641470.CrossRefGoogle ScholarPubMed
Whittington, J.E., Holland, A.J., Webb, T., Butler, J.V., Clarke, D.J., & Boer, H. (2004). Cognitive abilities and genotype in a population-based sample of people with Prader–Willi syndrome. Journal of Intellectual Disability Research, 48, 172187.CrossRefGoogle Scholar
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Whittington, J.E., Holland, A.J., & Webb, T. (2014). Ageing in people with Prader–Willi syndrome: Mortality in the UK population cohort and morbidity in an older sample of adults. Psychological Medicine, 45, 615621.CrossRefGoogle Scholar
Woodcock, K.A., Oliver, C., & Humphreys, G.W. (2009). 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. Cognitive Neuropsychology, 26, 172–94.CrossRefGoogle ScholarPubMed

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