학술논문

Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations
Document Type
Article
Author
Rebbeck, T.R.Friebel, T.M.Friedman, E.Laitman, Y.Hamann, U.Torres, D.Rashid, M.U.Huo, D.Olopade, O.I.Kwong, A.Olah, E.Papp, J.Solano, A.R.Teo, S.-H.Yoon, S.-Y.Thomassen, M.Kruse, T.A.Nielsen, H.R.Weitzel, J.N.Blazer, K.R.Slavin, T.P.Chan, T.L.Couch, F.J.Goldgar, D.E.Palmero, E.I.Park, S.K.van Rensburg, E.J.Dorfling, C.M.Parsons, M.T.Chenevix-Trench, G.Spurdle, A.B.Aalfs, C.M.Abugattas, J.Adlard, J.Agata, S.Montagna, M.Tognazzo, S.Aittomäki, K.Andrews, L.Andrulis, I.L.Arnold, N.Arun, B.K.Gutierrez-Barrera, A.Asseryanis, E.Auerbach, L.Berger, A.Singer, C.F.Tan, Y.Y.Azzollini, J.Manoukian, S.Zanzottera, C.Balmaña, J.Barile, M.Bonanni, B.Arason, A.Barkardottir, R.B.Benitez, J.Berger, R.Blanco, A.M.Blok, M.J.Bonadona, V.Lasset, C.Bradbury, A.R.Domchek, S.M.Shah, P.D.Nathanson, K.L.Brewer, C.Buecher, B.Caputo, S.M.de Pauw, A.Gauthier-Villars, M.Buys, S.S.Caldes, T.de la Hoya, M.Caliebe, A.Caligo, M.A.Campbell, I.Chiquette, J.Chung, W.K.Claes, K.B.M.De Leeneer, K.Van Heetvelde, M.Collée, J.M.Cook, J.Davidson, R.Delnatte, C.Diez, O.Ding, Y.C.Neuhausen, S.L.Steele, L.Ditsch, N.Velazquez, C.Dworniczak, B.Eason, J.Eeles, R.Ehrencrona, H.Ejlertsen, B.Engel, C.Engert, S.Meindl, A.Evans, D.G.Faivre, L.Feliubadaló, L.Lázaro, C.Ferrer, S.F.Foretova, L.Machackova, E.Fowler, J.Galvão, H.C.R.Ganz, P.A.Garber, J.Gehrig, A.Gerdes, A.-M.Gesta, P.Giannini, G.Giraud, S.Glendon, G.Godwin, A.K.Greene, M.H.Loud, J.T.Gronwald, J.Jakubowska, A.Kaczmarek, K.Lubinski, J.Peruga, N.Prajzendanc, K.Sukiennicki, G.Hahnen, E.Hauke, J.Pohl, E.Rhiem, K.Schmutzler, R.K.Wappenschmidt, B.Henderson, A.Hentschel, J.Hogervorst, F.B.L.van der Kolk, L.E.Honisch, E.Niederacher, D.Imyanitov, E.N.Isaacs, C.Izatt, L.Izquierdo, A.James, P.Janavicius, R.Jensen, U.B.Skytte, A.-B.John, E.M.Vijai, J.Musinsky, J.Pradhan, N.Topka, S.Karlan, B.Y.Lester, J.Kast, K.Kim, S.-W.Konstantopoulou, I.Yannoukakos, D.Korach, J.Lasa, A.Lee, A.Lee, M.H.Lesueur, F.Mebirouk, N.Liljegren, A.Lindor, N.M.Longy, M.Lu, K.H.Mari, V.Martínez-Bouzas, C.Matrai, Z.Meijers-Heijboer, H.E.J.Mensenkamp, A.R.Mickys, U.Miller, A.Moysich, K.B.Mulligan, A.M.Nevanlinna, H.Ngeow, J.Nguyen, H.P.Nielsen, F.C.Schmidt, A.Y.Nussbaum, R.L.Offit, K.Öfverholm, A.Ong, K.-R.Osorio, A.Papi, L.Pasini, B.Pedersen, I.S.Peixoto, A.Teixeira, M.R.Peterlongo, P.Prieur, F.Pujol, P.Radice, P.Ramus, S.J.Rantala, J.Robson, M.Rodriguez, G.C.Rogers, M.T.Rudaitis, V.Senter, L.Sharma, P.Side, L.E.Simard, J.Snape, K.Sobol, H.Southey, M.Steinemann, D.Sutter, C.Szabo, C.I.Terry, M.B.Teulé, A.Thomas, A.Thull, D.L.Tischkowitz, M.Toland, A.E.Trainer, A.H.Tung, N.van Asperen, C.J.van der Hout, A.H.van der Luijt, R.B.Varesco, L.Varon-Mateeva, R.Vega, A.Villarreal-Garza, C.von Wachenfeldt, A.Walker, L.Wang-Gohrke, S.Weber, B.H.F.Zidan, J.Zorn, K.K.Selkirk, C.G.H.Hulick, P.J.McGuffog, L.Leslie, G.Barrowdale, D.Easton, D.F.Frost, D.Antoniou, A.C.
Source
In: Human Mutation. (Human Mutation, May 2018, 39(5):593-620)
Subject
Language
English
ISSN
10981004
10597794