Treffer 1 - 20 von 26 für Suche 'Pauw, Eddy De', Suchdauer: 1,11s Treffer weiter einschränken
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    Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of B... von Mulligan, Anna Marie, Couch, Fergus J, Barrowdale, Daniel, Domchek, Susan M, Eccles, Diana, Nevanlinna, Heli, Ramus, Susan J, Robson, Mark, Sherman, Mark, Spurdle, Amanda B, Wappenschmidt, Barbara, Lee, Andrew, McGuffog, Lesley, Healey, Sue, Sinilnikova, Olga M, Janavicius, Ramunas, Hansen, Thomas vO, Nielsen, Finn C, Ejlertsen, Bent, Osorio, Ana, Muñoz-Repeto, Iván, Durán, Mercedes, Godino, Javier, Pertesi, Maroulio, Benítez, Javier, Peterlongo, Paolo, Manoukian, Siranoush, Peissel, Bernard, Zaffaroni, Daniela, Cattaneo, Elisa, Bonanni, Bernardo, Viel, Alessandra, Pasini, Barbara, Papi, Laura, Ottini, Laura, Savarese, Antonella, Bernard, Loris, Radice, Paolo, Hamann, Ute, Verheus, Martijn, Meijers-Heijboer, Hanne E J, Wijnen, Juul, Gómez García, Encarna B, Nelen, Marcel R, Kets, C Marleen, Seynaeve, Caroline, Tilanus-Linthorst, Madeleine M A, van der Luijt, Rob B, van Os, Theo, Rookus, Matti, Frost, Debra, Jones, J Louise, Evans, D Gareth, Lalloo, Fiona, Eeles, Ros, Izatt, Louise, Adlard, Julian, Davidson, Rosemarie, Cook, Jackie, Donaldson, Alan, Dorkins, Huw, Gregory, Helen, Eason, Jacqueline, Houghton, Catherine, Barwell, Julian, Side, Lucy E, McCann, Emma, Murray, Alex, Peock, Susan, Godwin, Andrew K, Schmutzler, Rita K, Rhiem, Kerstin, Engel, Christoph, Meindl, Alfons, Ruehl, Ina, Arnold, Norbert, Niederacher, Dieter, Sutter, Christian, Deissler, Helmut, Gadzicki, Dorothea, Kast, Karin, Preisler-Adams, Sabine, Varon-Mateeva, Raymonda, Schoenbuchner, Ines, Fiebig, Britta, Heinritz, Wolfram, Schäfer, Dieter, Gevensleben, Heidrun, Caux-Moncoutier, Virginie, Fassy-Colcombet, Marion, Cornelis, François, Mazoyer, Sylvie, Léoné, Mélanie, Boutry-Kryza, Nadia, Hardouin, Agnès, Berthet, Pascaline, Muller, Danièle, Fricker, Jean-Pierre, Mortemousque, Isabelle, Pujol, Pascal

    Veröffentlicht in Breast cancer research : BCR

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    Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers von Ramus, Susan J., Kuchenbaecker, Karoline B., Beesley, Jonathan, Healey, Sue, Thomassen, Mads, Jensen, Uffe Birk, Skytte, Anne-Bine, Lindblom, Annika, Olsson, Håkan, Melin, Beatrice, Domchek, Susan M., Nathanson, Katherine L., Jakubowska, Anna, Lubinski, Jan, Jaworska, Katarzyna, Durda, Katarzyna, Złowocka, Elżbieta, Gronwald, Jacek, Huzarski, Tomasz, Byrski, Tomasz, Benitez, Javier, Tejada, Maria-Isabel, Aalfs, Cora M., Meijers-Heijboer, Hanne E.J., van Asperen, Christi J., van Roozendaal, K.E.P., Collée, J. Margriet, van der Luijt, Rob B., Frost, Debra, Platte, Radka, Fineberg, Elena, Evans, D. Gareth, Lalloo, Fiona, Jacobs, Chris, Adlard, Julian, Davidson, Rosemarie, Cook, Jackie, Paterson, Joan, Morrison, Patrick J., Kennedy, M. John, Godwin, Andrew K., Caux-Moncoutier, Virginie, Gauthier-Villars, Marion, Mazoyer, Sylvie, Lasset, Christine, Hardouin, Agnès, Berthet, Pascaline, Faivre, Laurence, Buys, Saundra, Beth Terry, Mary, Chung, Wendy K., John, Esther M, Tea, Muy-Kheng, Pfeiler, Georg, Fink-Retter, Anneliese, Hansen, Thomas v. O., Ejlertsen, Bent, Offit, Kenneth, Gaudet, Mia M., Vijai, Joseph, Robson, Mark, Phillips, Kelly-Anne, Hoffman, James S, Montagna, Marco, Tognazzo, Silvia, Isaacs, Claudine, Janavicius, Ramunas, Blanco, Ignacio, Navarro, Matilde, Karlan, Beth Y., Olah, Edith, Vaszko, Tibor, Teo, Soo-Hwang, Ganz, Patricia A., Diez, Orland, Schmutzler, Rita K., Wappenschmidt, Barbara, Engel, Christoph, Meindl, Alfons, Arnold, Norbert, Niederacher, Dieter, Deissler, Helmut, Fiebig, Britta, Nevanlinna, Heli, Aittomäki, Kristiina, Plante, Marie, Spurdle, Amanda B., Ding, Yuan Chun, Lindor, Noralane, Fredericksen, Zachary, Pankratz, V. Shane, Peissel, Bernard, Bernard, Loris, Dolcetti, Riccardo, Radice, Paolo, Greene, Mark H., Mai, Phuong L., Ozcelik, Hilmi, Couch, Fergus J., Chenevix-Trench, Georgia

    Veröffentlicht in Human mutation

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