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    a likelihood ratio approach for utilizing case-control data in the clinical classification of rare sequence variants: application to BRCA1 and BRCA2 von O'Mahony, D.G., Parsons, M.T., Li, H.Y., Dennis, J., Aittomäkkiki, K., Andrulis, I.L., Anton-Culver, H., Aronson, K.J., Bojesen, S.E., Bolla, M.K., Brenner, H., Buys, S.S., Canzian, F., Caputo, S.M., Czene, K., Daly, M.B., Nicolo, A. de, Devilee, P., Dörk, T., Dunning, A.M., Dwek, M., Eccles, D.M., Engel, C., Evans, D.G., Fasching, P.A., Gago-Dominguez, M., García-Closas, M., García-Sáenz, J.A., Gentry-Maharaj, A., Geurts-Giele, W.R.R., Giles, G.G., Glendon, G., Goldberg, M.S., Garcia, E.B.G., Güendert, M., Guénel, P., Haiman, C.A., Hall, P., Hamann, U., Harkness, E.F., Hoppe, R., Hopper, J.L., Howell, A., Investigators, A., Jakimovska, M., Jakubowska, A., Jernström, H., Kaaks, R., Kitahara, C.M., Koutros, S., Kraft, P., Kristensen, V.N., Lambrechts, D., Léoné, M., Lindblom, A., Manoochehri, M., Manoukian, S., Margolin, S., Martinez, M.E., Menon, U., Milne, R.L., Neuhausen, S.L., Nevanlinna, H., Newman, W.G., Offit, K., Park, S.K., James, P., Peterlongo, P., Peto, J., Plaseska-Karanfilska, D., Punie, K., Radice, P., Rashid, M.U., Rennert, G., Rosenberg, E.H., Saloustros, E., Sandler, D.P., Schmidt, M.K., Schmutzler, R.K., Shu, X.O., Simard, J., Southey, M.C., Stone, J., Stoppa-Lyonnet, D., Tapper, W.J., Taylor, J.A., Teo, S.H., Teras, L.R., Terry, M.B., Vachon, C.M., Vega, A., Wang, Q., Weinberg, C.R., Wolk, A., Zheng, W., Couch, F.J., Spurdle, A.B., Easton, D.F., Goldgar, D.E., Michailidou, K.

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