P03.21 Casp9 germline mutation in a family with multiple brain tumors

Por Ronellenfitsch, M. W., Oh, J., Satomi, K., Sumi, K., Harter, P. N., Steinbach, J. P., Felsberg, J., Capper, D., Voegele, C., Schittenhelm, J., Mittelbronn, M., Ohgaki, H.
Publicado no Neuro Oncol (2017)

Rare Mutations in XRCC2 Increase the Risk of Breast Cancer

Por Park, D.J., Lesueur, F., Nguyen-Dumont, T., Pertesi, M., Odefrey, F., Hammet, F., Neuhausen, S.L., John, E.M., Andrulis, I.L., Terry, M.B., Daly, M., Buys, S., Le Calvez-Kelm, F., Lonie, A., Pope, B.J., Tsimiklis, H., Voegele, C., Hilbers, F.M., Hoogerbrugge, N., Barroso, A., Osorio, A., Giles, G.G., Devilee, P., Benitez, J., Hopper, J.L., Tavtigian, S.V., Goldgar, D.E., Southey, M.C.
Publicado em 2012

Multigene testing of moderate-risk genes: be mindful of the missense

Por Young, E L, Feng, B J, Stark, A W, Damiola, F, Durand, G, Forey, N, Francy, T C, Gammon, A, Kohlmann, W K, Kaphingst, K A, McKay-Chopin, S, Nguyen-Dumont, T, Oliver, J, Paquette, A M, Pertesi, M, Robinot, N, Rosenthal, J S, Vallee, M, Voegele, C, Hopper, J L, Southey, M C, Andrulis, I L, John, E M, Hashibe, M, Gertz, J, Le Calvez-Kelm, F, Lesueur, F, Goldgar, D E, Tavtigian, S V
Publicado no J Med Genet (2016)