1. Adelaide Research & Scholarship

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Results 31-40 of 51 (Search time: 0.004 seconds).
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PreviewIssue DateTitleAuthor(s)
2004Phenotypic variability: Clinical presentation between the 6th year and the 60th year in a family with X-linked agammaglobulinemiaMorwood, K.; Bourne, H.; Philpot, R.; Gold, M.; Gillis, D.; Benson, E.
2005Enzyme replacement therapy for Gaucher disease in AustraliaGoldblatt, J.; Szer, J.; Fletcher, J.; McGill, J.; Rowell, J.; Wilson, M.
2007A cross-sectional survey to assess community attitudes to introduction of human papillomavirus vaccineMarshall, H.; Ryan, P.; Roberton, D.; Baghurst, P.
2008Familial 22q11.2 duplication: a three-generation family with a 3-Mb duplication and a familial 1.5-Mb duplicationYu, S.; Cox, K.; Friend, K.; Smith, S.; Buchheim, R.; Bain, S.; Leibelt, J.; Thompson, E.; Bratkovic, D.
2007Promoting lay participation in medical school curriculum development: Lay and faculty perspectivesO'Keefe, M.; Jones, A.
2007Immunomodulatory constituents of human milk change in response to infant bronchiolitisBryan, D.; Hart, P.; Forsyth, K.; Gibson, R.
2005The Hunter-McAlpine syndrome results from duplication 5q35-qterHunter, A.; DuPont, B.; McLaughlin, M.; Hinton, L.; Baker, E.; Ades, L.; Haan, E.; Schwartz, C.
2008Human nocturnal frontal lobe epilepsy: Pharmocogenomic profiles of pathogenic nicotinic acetylcholine receptor β-subunit mutations outside the ion channel poreHoda, J.; Gu, W.; Friedli, M.; Phillips, H.; Bertrand, S.; Antonarakis, S.; Goudie, D.; Roberts, R.; Scheffer, I.; Marini, C.; Patel, J.; Berkovic, S.; Mulley, J.; Steinlein, O.; Bertrand, D.
2007Unravelling the molecular control of calvarial suture fusion in children with craniosynostosisCoussens, A.; Wilkinson, C.; Hughes, I.; Morris, C.; Van Daal, A.; Anderson, P.; Powell, B.
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.

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