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Results 31-39 of 39 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
2009SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotypeSpurlock, G.; Bennett, E.; Chuzhanova, N.; Thomas, N.; H-Ping, J.; Side, L.; Davies, S.; Haan, E.; Kerr, B.; Huson, S.; Upadhyaya, M.
2004Mutations of the mitochondrial ND1 gene as a cause of MELASKirby, D.; McFarland, R.; Ohtake, A.; Dunning, C.; Ryan, M.; Wilson, C.; Ketteridge, D.; Turnbull, D.; Thorburn, D.; Taylor, R.
2000Childhood cancer: A 4-year prospective study of the psychological adjustment of children and parentsSawyer, M.; Antoniou, G.; Toogood, I.; Rice, M.; Baghurst, P.
2009Adenotonsillectomy and neurocognitive deficits in children with sleep disordered breathingKohler, M.; Lushington, K.; van den Heuvel, C.; Martin, A.; Pamula, Y.; Kennedy, J.; Rogers, N.
2009A Novel Bocavirus Associated with Acute Gastroenteritis in Australian ChildrenArthur, J.; Higgins, G.; Davidson, G.; Givney, R.; Ratcliff, R.; Münger, K.
2002Generalized epilepsy with febrile seizures plus: Mutation of the sodium channel subunit SCN1BWallace, R.; Scheffer, I.; Parasivam, G.; Barnett, S.; Wallace, G.; Sutherland, G.; Berkovic, S.; Mulley, J.
2009Weight gain in early life predicts risk of islet autoimmuity in children with a first-degree relative with type 1 diabetesCouper, J.; Beresford, S.; Hirte, C.; Baghurst, P.; Pollard, A.; Tait, B.; Harrison, L.; Colman, P.
2000Reflux in childrenDavidson, G.; Omari, T.
2008Perinatal and paediatric pathology special theme issueDahlstrom, J.E.; Khong, T.Y.

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