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Browsing by Author Grist, Scott Andrew

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PreviewIssue DateTitleAuthor(s)
2009Analysis of a set of missense, frameshift, and in-frame deletion variants of BRCA1Grist, Scott Andrew; Beddor, J; Pino, MA; Carvalho, M; Mesquita, RD; Billack, B; Karchin, R; Godinho-Netto, M; Rodarte, RS; Colombo, M; Ripamonti, CB; Rosenquist, R; Suthers, Graeme; Radice, P; Monteiro, AN; Monteiro, VA; Manoukian, S; Borg, A
2007Determination of cancer risk associated with germ line BRCA1 missense variants by functional analysisCarvalho, Marcelo; Couch, Fergus; Radice, Paolo; Monteiro, Alvaro; Karchin, Rachel; Grist, Scott Andrew; Gayol, Luis; Sali, Andrej; Goldgar, David; Marsillac, Sylvia; Baumbach, Lisa; Sutphen, Rebecca; Pickard-Brzosowicz, Jennifer; Manoukian, Siranoush; Swaby, Ramona; Silva, Rosane; Urmenyi, Turan; Rondinelli, Edson; Nathanson, Katherine
2007Functional characterization of human MutY homolog (hMYH) missense mutation (R231L) that is linked with hMYH-associated polyposisSuthers, Graeme; Wilson, Teresa; Lu, A-Lien; Grist, Scott Andrew; Gardner, Justin; Bai, Haibo
2004Mitochondrial mutations in acute leukemiaGrist, Scott Andrew; Lu, X; Morley, Alexander Alan
2008Pathogenicity of the BRCA1 missense variant M1775K is determined by the disruption of the BRCT phosphopeptide-binding pocket: a multi-modal approachTischkowitz, Marc; Hamel, Nancy; Carvalho, Marcelo; Birrane, Gabriel; Soni, Aditi; van Beers, Erik H; Joosse, Simon A; Wong, Nora; Quenneville, Louise A; Grist, Scott Andrew; ConFab Investigators; Nederlof, Petra; Goldgar, David; Tavtigian, Sean V; Monteiro, Alvaro; Ladias, John A; Foulkes, William D; Novak, David
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