https://ogma.newcastle.edu.au/vital/access/ /manager/Index ${session.getAttribute("locale")} 5 Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:10275 Sat 24 Mar 2018 08:13:04 AEDT ]]> Associations Between Hyperphagia, Symptoms of Sleep Breathing Disorder, Behaviour Difficulties and Caregiver Well-Being in Prader-Willi Syndrome: A Preliminary Study https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:44807 Mon 24 Oct 2022 09:31:54 AEDT ]]> Daytime sleepiness and emotional and behavioral disturbances in Prader-Willi syndrome https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:52313 Mon 09 Oct 2023 10:23:33 AEDT ]]> Requirements for improving health and well-being of children with Prader-Willi syndrome and their families https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:45712 Fri 04 Nov 2022 10:23:59 AEDT ]]>