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Results 1-10 of 11 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2013Paediatric active enhanced disease surveillance: a new surveillance system for AustraliaZurynski, Y.; McIntyre, P.; Booy, R.; Elliott, E.; PAEDS Investigators Group.; Marshall, Helen Siobhan
2013International collaboration to assess the risk of Guillain Barré Syndrome following Influenza A (H1N1) 2009 monovalent vaccinesDodd, Caitlin N.; ... et al.; Global H1N1 GBS Consortium; Marshall, Helen Siobhan
2014Nonsense-mediated mRNA decay: Inter-individual variability and human diseaseNguyen, L.; Wilkinson, M.; Gecz, J.
2013The UPF3B gene, implicated in intellectual disability, autism, ADHD and childhood onset schizophrenia regulates neural progenitor cell behaviour and neuronal outgrowthJolly, L.; Homan, C.; Jacob, R.; Barry, S.; Gecz, J.
2014Parental and community acceptance of the benefits and risks associated with meningococcal B vaccinesMarshall, H.; Clarke, M.; Sullivan, T.
2014Placental restriction of fetal growth reduces cutaneous responses to antigen after sensitization in sheepWooldridge, A.; Bischof, R.; Meeusen, E.; Liu, H.; Heinemann, G.; Hunter, D.; Giles, L.; Kind, K.; Owens, J.; Clifton, V.; Gatford, K.
2012New mutations and sporadic intellectual disabilityGecz, J.; Haan, E.
2014UPF3B gene and nonsense-mediated mRNA decay in autism spectrum disordersLaumonnier, F.; Nguyen, L.; Jolly, L.; Raynaud, M.; Gecz, J.
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.
2014Phenotype-genotype complexities: opening DOORSBerkovic, S.; Gecz, J.