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TypeTitleAuthor(s)YearViews
ENIGMA - evidence-based network for the interpretation of germline mutant alleles: an international initiative to evaluate risk and clinical significance associated with sequence variation in BRCA1 and BRCA2 genes
Journal:
Human Mutation
Spurdle, AB; Healey, S; Devereau, A; Hogervorst, FB; Monteiro, AN; Nathanson, KL; Radice, P; Stoppa-Lyonnet, D; Tavtigian, S; Wappenschmidt, B; Couch, FJ; Pertesi, M; Cornell, M; Rouleau, E; Sharan, S; Rahman, N; Lalloo, F; Weitzel, J; Campbell, J; Cummings,; Machakova, E; Goldgar, DE; Olopade, F; Godwin, A; Ozcelik, H; Seminara, D; Goldgar, D; Couch, F; Fackenthal, JD; Thomassen, M; Teo, SH; Hansen, TV; Borg, A; Eeles, R; Toland, A; Rogan, P; Hansen, TV; Guidugli, L; Brody, LC; Healey, S; Brown, M; Kwong, A; Lei-po, CW; Nevanlinna, H; Garber, J; Foretova, L; Singer, CF; Blok, MJ; Spurdle, AB; Osorio, A; Kote-Jarai, Z; Wappenschmidt, B; Baralle, D; Vega, A; Blanco, A; Santamarina, M; Fachal, L; Nederlof, P; Peock, S; Pasini, B; Tommasi, S; Lafferty, A; Arisari, A; Konstantopoulou, I; Pal, T; Simard, J; Bonetti, A; Voresco, L; Peissel, B; Evans, DG; Foulkes, W; Szabo, C; van Asperen, C; Jonkers, J; Walker, L; Mitchell, G; Gutierrez-Enriquez, S; Diez, O; Millot, G; Fostira, F; Selkirk, C; Antoniou, A; Monteiro, A; Carvalho, M; Rubinstein, WS; de la Hoya, M; Domchek, S; Caputo, S; Houdayer, C; Blanco, I; Lazaro, C; Whiley, P; Becker, A; Aretini, P; Eccles, D; Caides, T; Viel, A; Izatt, L; Hogervorst, F; Radice, P; Nathanson, K; Pedersen, IS; Vreeswijk, M; Neuhausen, S; Yannoukakos, K; Tucker, K; Southey, M; Leary, J; Caligo, MA; Garcia, EG; Devereau, A; Brandao, R; Lidereau, R; Montagna, M2012268
 
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