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PreviewIssue DateTitleAuthor(s)
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.
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.
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.
2007Inheritance of a cancer-associated MLH1 germ-line epimutationHitchins, M.; Wong, J.; Suthers, G.; Suter, C.; Martin, D.; Hawkins, N.; Ward, R.
2009Analysis of a set of missense, frameshift, and in-frame deletion variants of BRCA1Carvalho, M.; Pino, M.; Karchin, R.; Beddor, J.; Godinho-Netto, M.; Mesquita, R.; Rodarte, R.; Vaz, D.; Monteiro, V.; Manoukian, S.; Colombo, M.; Ripamonti, C.; Rosenquist, R.; Suthers, G.; Borg, A.; Radice, P.; Grist, S.; Monteiro, A.; Billack, B.
2012Gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS): A new autosomal dominant syndromeWorthley, D.; Phillips, K.; Wayte, N.; Schrader, K.; Healey, S.; Kaurah, P.; Shulkes, A.; Grimpen, F.; Clouston, A.; Moore, D.; Cullen, D.; Ormonde, D.; Mounkley, D.; Wen, X.; Lindor, N.; Carniero, F.; Huntsman, D.; Chenevix-Trench, G.; Suthers, G.
2005MLH1 germline epimutations as a factor in hereditary nonpolyposis colorectal cancerHitchins, M.; Williams, R.; Cheong, K.; Halani, N.; Lin, V.; Packham, D.; Ku, S.; Buckle, A.; Hawkins, N.; Burn, J.; Gallinger, S.; Goldblatt, J.; Kirk, J.; Tomlinson, I.; Scott, R.; Spigelman, A.; Suter, C.; Martin, D.; Suthers, G.; Ward, R.

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