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PreviewIssue DateTitleAuthor(s)
2000Attitudes to genetic testing for breast cancer susceptibility in women at increased risk of developing hereditary breast cancerMeiser, B.; Butow, P.; Barratt, A.; Suthers, G.; Smith, M.; Colley, A.; Thompson, E.; Tucker, K.
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.
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.
2007Inheritance of a cancer-associated MLH1 germ-line epimutationHitchins, M.; Wong, J.; Suthers, G.; Suter, C.; Martin, D.; Hawkins, N.; Ward, R.
2010Lynch syndrome-associated breast cancers: Clinicopathologic characteristics of a case series from the colon cancer family registryWalsh, M.; Buchanan, D.; Cummings, M.; Pearson, S.; Arnold, S.; Clendenning, M.; Walters, R.; McKeone, D.; Spurdle, A.; Hopper, J.; Jenkins, M.; Phillips, K.; Suthers, G.; George, J.; Goldblatt, J.; Muir, A.; Tucker, K.; Pelzer, E.; Gattas, M.; Woodall, S.; et al.
2008Methionine-dependence phenotype in the de novo pathway in BRCA1 and BRCA2 mutation carriers with and without breast cancerBeetstra, S.; Suthers, G.; Dhillon, V.; Salisbury, C.; Turner, J.; Altree, M.; McKinnon, R.; Fenech, M.

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