https://ogma.newcastle.edu.au/vital/access/ /manager/Index ${session.getAttribute("locale")} 5 Deep phenotyping of the neuroimaging and skeletal features in KBG syndrome: a study of 53 patients and review of the literature https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:54396 Wed 21 Feb 2024 15:34:25 AEDT ]]> Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:21181 Wed 11 Apr 2018 14:28:23 AEST ]]>