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PreviewIssue DateTitleAuthor(s)
2010Association between erythropoietin gene polymorphisms and diabetic retinopathyAbhary, S.; Burdon, K.; Casson, R.; Goggin, M.; Petrovsky, N.; Craig, J.
2010Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genesDimasi, D.; Chen, J.; Hewitt, A.; Klebe, S.; Davey, R.; Stirling, J.; Thompson, E.; Forbes, R.; Tan, T.; Savarirayan, R.; Mackey, D.; Healey, P.; Mitchell, P.; Burdon, K.; Craig, J.
2010DNA methylation-mediated Down-regulation of DNA methyltransferase-1 (DNMT1) is coincident with, but not essential for, global hypomethylation in human placentaNovakovic, B.; Wong, N.; Sibson, M.; Ng, H.; Morley, R.; Manuelpillai, U.; Down, T.; Rakyan, V.; Beck, S.; Hiendleder, S.; Roberts, C.; Craig, J.; Saffery, R.
2010Opinions on the content and effects of the Caring for Australasians with Renal Impairment (CARI) Guidelines: A survey of renal nurses and comparison with the opinions of nephrologists in AustralasiaIrving, M.; Johnson, D.; McDonald, S.; Walker, R.; Frommer, M.; Fetherstonhaugh, D.; Deans, P.; Craig, J.
2010A novel syndrome of paediatric cataract, dysmorphism, ectodermal features, and developmental delay in Australian Aboriginal family maps to 1p35.3-p36.32Hattersley, K.; Laurie, K.; Liebelt, J.; Gecz, J.; Durkin, S.; Craig, J.; Burden, K.
2010Aldose reductase gene polymorphisms and diabetic retinopathy susceptibilityAbhary, S.; Burdon, K.; Laurie, K.; Thorpe, S.; Landers, J.; Goold, L.; Lake, S.; Petrovsky, N.; Craig, J.

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