Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/32928
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Type: Journal article
Title: Prader-Willi Syndrome
Author: Couper, R.
Couper, J.
Citation: The Lancet, 2000; 356(9230):673-675
Publisher: Lancet Ltd
Issue Date: 2000
ISSN: 0140-6736
1474-547X
Keywords: Chromosomes, Human, Pair 15
Humans
Prader-Willi Syndrome
Muscle Hypotonia
Hypogonadism
Hyperphagia
Genomic Imprinting
Adult
Female
Intellectual Disability
DOI: 10.1016/S0140-6736(00)02617-9
Published version: http://dx.doi.org/10.1016/s0140-6736(00)02617-9
Appears in Collections:Aurora harvest
Paediatrics publications

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