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PreviewIssue DateTitleAuthor(s)
2008A novel locus for X-linked congenital cataract on Xq24Craig, J.; Friend, K.; Gecz, J.; Rattray, K.; Trotski, M.; Mackey, D.; Burdon, K.
2008SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndromeGilfillan, G.; Selmer, K.; Roxrud, I.; Smith, R.; Kyllerman, M.; Eiklid, K.; Kroken, M.; Mattingsdal, M.; Egeland, T.; Stenmark, H.; Sjoholm, H.; Server, A.; Samuelsson, L.; Christianson, A.; Tarpey, P.; Whibley, A.; Stratton, M.; Futreal, P.; Teague, J.; Edkins, S.; et al.
2008Glucose control, organ failure, and mortality in pediatric intensive careYung, M.; Wilkins, B.; Norton, L.; Slater, A.
2008Videomanometric evaluation of pharyngo-oesophageal dysmotility in children with velocardiofacial syndromeRommel, N.; Davidson, G.; Cain, T.; Hebbard, G.; Omari, T.
2008Self-Esteem, Self-Concept, and Quality of Life in Children with Hemiplegic Cerebral PalsyRusso, R.; Goodwin, E.; Miller, M.; Haan, E.; Connell, T.; Crotty, M.
2008Long-term follow-up of endurance and safety outcomes during enzyme replacement therapy for mucopolysaccharidosis VI: Final results of three clinical studies of recombinant human N-acetylgalactosamine 4-sulfataseHarmatz, P.; Giugliani, R.; Schwartz, I.; Guffon, N.; Teles, E.; Miranda, C.; Wraith, J.; Beck, M.; Arash, L.; Scarpa, M.; Ketteridge, D.; Hopwood, J.; Plecko, B.; Steiner, R.; Whitley, C.; Kaplan, P.; Yu, Z.; Swiedler, S.; Decker, C.
2008Comorbities of overweight/obesity in Australian preschoolers: a cross-sectional population studyWake, M.; Hardy, P.; Sawyer, M.; Carlin, J.
2008Somatic mutations in GLI3 can cause hypothalamic hamartoma and gelastic seizuresWallace, R.; Freeman, J.; Shouri, M.; Izzillo, P.; Rosenfield, J.; Mulley, J.; Harvey, A.; Berkovic, S.
2008Perinatal and paediatric pathology special theme issueDahlstrom, J.E.; Khong, T.Y.

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