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PreviewIssue DateTitleAuthor(s)
2000WISDOM Will Australian women participate?MacLennan, A.; Paine, B.; Marley, J.
2002Projections of Australian obstetricians ceasing practice and the reasonsMacLennan, A.; Spencer, M.
2001A single nucleotide polymorphism in the 5' untranslated region of RAD51 and risk of cancer among BRCA1/2 mutation carriersWang, W.; Spurdle, A.; Kolachana, P.; Bove, B.; Modan, B.; Ebbers, S.; Suthers, G.; Tucker, M.; Kaufman, D.; Doody, M.; Tarone, R.; Daly, M.; Levavi, H.; Pierce, H.; Chetrit, A.; Yechezkel, G.; Chenevix-Trench, G.; Offit, K.; Godwin, A.; Struewing, J.
1998Evaluation of the lysosome-associated membrane protein LAMP-2 as a marker for lysosomal storage disordersHua, C.; Hopwood, J.; Carlsson, S.; Harris, R.; Meikle, P.
2014Tumor mismatch repair immunohistochemistry and DNA MLH1 methylation testing of patients with endometrial cancer diagnosed at age younger than 60 years optimizes triage for population-level germline mismatch repair gene mutation testingBuchanan, D.; Tan, Y.; Walsh, M.; Clendenning, M.; Metcalf, A.; Ferguson, K.; Arnold, S.; Thompson, B.; Lose, F.; Parsons, M.; Walters, R.; Pearson, S.; Cummings, M.; Oehler, M.; Blomfield, P.; Quinn, M.; Kirk, J.; Stewart, C.; Obermair, A.; Young, J.; et al.
2014Survival of Australian women with invasive epithelial ovarian cancer: a population-based studyAnuradha, S.; Webb, P.; Blomfield, P.; Brand, A.; Friedlander, M.; Leung, Y.; Obermair, A.; Oehler, M.; Quinn, M.; Steer, C.; Jordan, S.
2002The prevalence of recalled low back pain during and after pregnancy: a South Australian population surveyStapleton, D.; MacLennan, A.; Kristiansson, P.
2001Long-term outcomes of genetic counseling in women at increased risk of developing hereditary breast cancerMeiser, B.; Butow, P.; Barratt, A.; Schneiden, V.; Gattas, M.; Kirk, J.; Gaff, C.; Suthers, G.; Tucker, K.
2009Cohort Profile: The North West Adelaide Health Study (NWAHS)Grant, J.; Taylor, A.; Ruffin, R.; Wilson, D.; Phillips, P.; Adams, R.; Price, K.
2010Risks of Lynch Syndrome cancers for MSH6 mutation carriersSuthers, G.