1. Adelaide Research & Scholarship

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Results 1-10 of 61 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2004Tissue plasminogen activator-7351C/T enhancer polymorphism is a risk factor for lacunar strokeJannes, J.; Hamilton-Bruce, M.; Pilotto, L.; Smith, B.; Mullighan, C.; Bardy, P.; Koblar, S.
2013Contraception and abortion in a low-fertility setting: the role of seasonal migrationSevoyan, A.; Agadjanian, V.
2007Trends in cancer mortality during the 20th century in AustraliaFreak-Poli, R.; Bi, P.; Hiller, J.
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.
2006Positive and negative affect and oral health-related quality of lifeBrennan, D.; Singh, K.; Spencer, A.; Roberts-Thomson, K.
1989Pontomedullary tears and other gross brainstem injuries after vehicular accidentsSimpson, D.; Blumbergs, P.; Cooter, R.; Kilminster, M.; McLean, J.; Scott, G.
2006Practice profiles of Australian private general dental practitionersBrennan, D.; Spencer, A.
1994Brain injury patterns in fatally injured pedestriansRyan, G.; McLean, J.; Kloeden, C.; Vilenius, A.; Simpson, D.; Blumbergs, P.; Scott, G.
2010Depression and obesity in adults with asthma: multiple comorbidities and management issuesWilson, D.; Appleton, S.; Taylor, A.; Tucker, G.; Ruffin, R.; Wittert, G.; Hugo, G.; Goldney, R.; Findlay, C.; Adams, R.
2007Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardationTarpey, P.; Raymond, F.; Nguyen, L.; Rodriguez, J.; Hackett, A.; Vandeleur, L.; Smith, R.; Shoubridge, C.; Edkins, S.; Stevens, C.; O'Meara, S.; Tofts, C.; Barthorpe, S.; Buck, G.; Cole, J.; Halliday, K.; Hills, K.; Jones, D.; Mironenko, T.; Perry, J.; et al.

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