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Results 1-10 of 18 (Search time: 0.003 seconds).
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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.
1997Most germ-line mutations in the nevoid basal cell carcinoma syndrome lead to a premature termination of the PATCHED protein, and no genotype-phenotype correlations are evidentWicking, C.; Shanley, S.; Smyth, I.; Gillies, S.; Negus, K.; Graham, S.; Suthers, G.; Haites, N.; Edwards, M.; Wainwright, B.; Chenevix Trench, G.
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.
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.
2000Intention to undergo prophylactic bilateral mastectomy in women at increased risk of developing hereditary breast cancerMeiser, B.; Butow, P.; Friedlander, M.; Schnieden, V.; Gattas, M.; Kirk, J.; Suthers, G.; Haan, E.; Tucker, K.
1997Mutation detection in FGFR2 craniosynostosis syndromesHollway, G.; Suthers, G.; Haan, E.; Thompson, E.; David, D.; Gecz, J.; Mulley, J.
2005Ratio of male to female births in the offspring of BRCA1 and BRCA2 carriersChenevix-Trench, G.; Sinilnikova, O.; Suthers, G.; Pandeya, N.; Mazoyer, S.; Sambrook, J.; Goldup, S.; Goldgar, D.; Lynch, H.; Lenoir, G.; Cheetham, G.
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.
2010Risks of Lynch Syndrome cancers for MSH6 mutation carriersSuthers, G.
2000Microsatellite instability markers in breast cancer: A review and study showing MSI was not detected at 'BAT 25' and 'BAT 26' microsatellite markers in early-onset breast cancerSiah, S.; Quinn, D.; Bennet, G.; Casey, G.; Flower, R.; Suthers, G.; Rudzki, Z.