The exon 13 duplication in the BRCA1 gene is a founder mutation present in geographicaly diverse populations

S. Mazoyer, J. Leary, J. Kirk, E. Fleischmann, T. Wagner, K. Claes, L. Messiaen, W. Foulkes, M. Desrochers, J. Simard, C. M. Phelan, E. Kwan, S. A. Narod, P. Vahteristo, H. Nevanlinna, X. Durando, Y. J. Bignon, J. P. Peyrat, C. Bonnardel, O. M. SinilnikovaN. Puget, G. M. Lenoir, C. Audoynaud, D. Goldgar, C. Maugard, V. Caux, S. Gad, D. Stoppa-Lyonnet, C. Noguès, R. Lidereau, C. Machavoine, B. Bressac-De Paillerets, B. Kuschel, B. Betz, D. Niederacher, M. W. Beckmann, U. Hamann, S. A. Gayther, B. A P Ponder, M. Robinson, G. R. Taylor, T. Bishop, A. Catteau, E. Solomon, B. Cohen, M. Steel, N. Collins, M. Stratton, M. Van Der Looij, E. Oláh, N. J. Miller, D. E. Barton, R. S. Sverdlov, E. Friedman, P. Radice, M. Montagna, E. Sensi, M. Caligo, R. Van Eijk, P. Devilee, R. Van Der Luijt, K. Heimdal, P. Møller, Å Borg, O. Diez, J. Cortes, M. Domenech, M. Baiget, A. Osorio, J. Benítez, P. Maillet, A. P. Sappino, H. Özdag, T. Özçelik, M. Ozturk, E. M. Rohlfs, J. Boyd, D. McDermott, K. Offit, M. Unger, K. Nathanson, B. L. Weber, T. A. Sellers, E. Hampton, F. J. Couch, S. Neuhausen

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