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    PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS von Southey, Melissa C, Winqvist, Robert, Pylkäs, Katri, Tischkowitz, Marc, Dennis, Joe, Michailidou, Kyriaki, Nevanlinna, Heli, Dörk, Thilo, Radice, Paolo, Carpenter, Jane, Fasching, Peter A, Haeberle, Lothar, Peto, Julian, dos-Santos-Silva, Isabel, Johnson, Nichola, Tomlinson, Ian, Marme, Federik, Truong, Thérèse, Neuhausen, Susan, Clarke, Christina A, Stegmaier, Christa, Brauch, Hiltrud, Brüning, Thomas, Ko, Yon-Dschun, Antonenkova, Natalia N, Kataja, Vesa, Wauters, Els, Smeets, Dominiek, Rudolph, Anja, Seibold, Petra, Pankratz, Vernon S, Le Marchand, Loic, Lindstrom, Sara, Glendon, Gord, Kauppila, Saila, Devilee, Peter, Hollestelle, Antoinette, Garcia-Closas, Montserrat, Figueroa, Jonine, Eriksson, Mikael, Hooning, Maartje J, Collée, J Margriet, Hall, Per, Dunning, Alison M, Hamann, Ute, Durda, Katarzyna, Yannoukakos, Drakoulis, Swerdlow, Anthony, Orr, Nick, González-Neira, Anna, Vincent, Daniel, Gronberg, Henrik, Travis, Ruth C, Hamdy, Freddie C, Cannon-Albright, Lisa, Butterbach, Katja, Batra, Jyotsna, Kote-Jarai, Zsofia, Wang-Gohrke, Shan, Sucheston-Campbell, Lara E, Friel, Grace, Lurie, Galina, Killeen, Jeffrey L, Goodman, Marc T, Butzow, Ralf, Modugno, Francesmary, Lester, Jenny, Peissel, Bernard, Bonanni, Bernardo, Bernard, Loris, Goode, Ellen L, Fogarty, Zachary C, Kalli, Kimberly R, Hildebrandt, Michelle A T, Iversen, Edwin S, Marks, Jeffrey R, Terry, Kathryn L, Poole, Elizabeth M, Stampfer, Meir, Orlow, Irene, Olson, Sara H, Massuger, Leon F A G, Brooks-Wilson, Angela, Le, Nhu D, Nedergaard, Lotte, Engelholm, Svend Aage, Siddiqui, Nadeem, Rothstein, Joseph H, Shu, Xiao-Ou, Sutphen, Rebecca, Narod, Steven A, Monteiro, Alvaro N, Chen, Y Ann, Tsai, Ya-Yu, Gentry-Maharaj, Aleksandra, Ramus, Susan J, Menon, Usha, Moes-Sosnowska, Joanna, Giles, Graham G, Tavtigian, Sean V

    Veröffentlicht in Journal of medical genetics

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