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Results 11-20 of 191 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2004TM4SF10 gene sequencing in XLMR patients identifies common polymorphisms but no disease-associated mutationChristophe-Hobertus, C.; Kooy, F.; Gecz, J.; Abramowicz, M.; Holinski-Feder, E.; Schwartz, C.; Christophe, D.
2008A novel locus for X-linked congenital cataract on Xq24Craig, J.; Friend, K.; Gecz, J.; Rattray, K.; Trotski, M.; Mackey, D.; Burdon, K.
2008Current use of Australian snake antivenoms and frequency of immediate-type hypersensitivity reactions and anaphylaxisIsbister, G.; Brown, S.; MacDonald, E.; White, J.; Currie, B.
2000New mutations in MID1 provide support for loss of function as the cause of X-linked Optiz syndromeCox, T.; Allen, L.; Cox, L.; Hopwood, B.; Goodwin, B.; Haan, E.; Suthers, G.
2006A pilot study of SRL 172 (killed Mycobacterium vaccae) in healthy chronic hepatitis B carriers and hepatitis B vaccine non-respondersGoldwater, P.
2009Effects of alcohol and sleep restriction on simulated driving performance in untreated patients with obstructive sleep apneaVakulin, A.; Baulk, S.; Catcheside, P.; Antic, N.; van den Heuvel, C.; Dorrian, J.; McEvoy, R.
2001The mental health of young people in Australia: key findings from the child and adolescent component on the national survey of mental health and well-beingSawyer, M.; Arney, F.; Baghurst, P.; Clark, J.; Graetz, B.; Kosky, R.; Nurcombe, B.; Patton, G.; Prior, M.; Raphael, B.; Rey, J.; Whaites, L.; Zubrick, S.
2004De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiencyMcFarland, R.; Kirby, D.; Fowler, K.; Ohtake, A.; Ryan, M.; Amor, D.; Fletcher, J.; Dixon, J.; Collins, F.; Turnbull, D.; Taylor, R.; Thorburn, A.
2005The effect of maternal asthma on placental and cord blood protein profilesMurphy, V.; Johnson, R.; Wang, Y.; Akinsanya, K.; Gibson, P.; Smith, R.; Clifton, V.
2009ASPREN surveillance system for influenza-like illness: a comparison with FluTracking and the National Notifiable Diseases Surveillance SystemParrella, A.; Dalton, C.B.; Pearce, R.; Litt, J.C.B.; Stocks, N.

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