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Results 1-10 of 93 (Search time: 0.004 seconds).
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PreviewIssue DateTitleAuthor(s)
2013RAB40AL loss-of-function mutation does not cause X-linked intellectual disabilityKalscheuer, V.; Iqbal, Z.; Hu, H.; Haas, S.; Shaw, M.; Lebrun, N.; Seemanova, E.; Voesenek, K.; Hobson, L.; Ropers, H.H.; Townshend, S.; Raynaud, M.; van Bokhoven, H.; Riazuddin, S.; Chelly, J.; Gecz, J.
2014Nonsense-mediated mRNA decay: Inter-individual variability and human diseaseNguyen, L.; Wilkinson, M.; Gecz, J.
2010Pharmacists' role in targeted cancer therapy in Australia and implications for pharmacy educationPlevin, D.; Ward, H.; Ward, M.; Sorich, M.; McKinnon, R.
1997Cloning and analysis of the human complement factor H gene promoterWard, H.; Higgs, N.; Blackmore, T.; Sadlon, T.
1998M protein of the group A streptococcus binds to the seventh short consensus repeat of human complement factor HBlackmore, T.; Fischetti, V.; Sadlon, T.; Ward, H.; Gordon, D.
1998Identification of a second heparin binding domain in human complement factor HBlackmore, T.; Hellwage, J.; Sadlon, T.; Higgs, N.; Zipfel, P.; Ward, H.; Gordon, D.
1996Identification of a heparin binding domain in the seventh short consensus repeat of complement factor HBlackmore, T.; Sadlon, T.; Ward, H.; Lublin, D.; Gordon, D.
2014UPF3B gene and nonsense-mediated mRNA decay in autism spectrum disordersLaumonnier, F.; Nguyen, L.; Jolly, L.; Raynaud, M.; Gecz, J.
2013Exploration and confirmation of factors associated with uncomplicated pregnancy in nulliparous women: prospective cohort studyChappell, L.; Seed, P.; Myers, J.; Taylor, R.; Kenny, L.; Dekker, G.; Walker, J.; McCowan, L.; North, R.; Poston, L.
2013Paediatric active enhanced disease surveillance: a new surveillance system for AustraliaZurynski, Y.; McIntyre, P.; Booy, R.; Elliott, E.; PAEDS Investigators Group.; Marshall, Helen Siobhan

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