Treffer 1 - 20 von 331 für Suche 'Gutiérrez, Angelica Y.', Suchdauer: 1,56s Treffer weiter einschränken
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    Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations von Rebbeck, Timothy R., Hamann, Ute, Olah, Edith, Solano, Angela R., Teo, Soo‐Hwang, Chan, TL, Couch, Fergus J., Palmero, Edenir Inêz, Park, Sue Kyung, Parsons, Michael T., Leslie, Goska, Aalfs, Cora M., Adlard, Julian, Agata, Simona, Aittomäki, Kristiina, Andrulis, Irene L., Barkardottir, Rosa B., Benitez, Javier, Blanco, Amie M., Bonadona, Valérie, Bonanni, Bernardo, Caligo, Maria A., Campbell, Ian, Chung, Wendy K., Claes, Kathleen B.M., Cook, Jackie, Davidson, Rosemarie, Leeneer, Kim, Domchek, Susan M., Dorfling, Cecilia M., Velazquez, Carolina, Easton, Douglas F., Feliubadaló, Lidia, Ferrer, Sandra Fert, Foretova, Lenka, Galvão, Henrique C. R., Garber, Judy, Gesta, Paul, Giannini, Giuseppe, Gutierrez‐Barrera, Angelica, Hogervorst, Frans B.L., Imyanitov, Evgeny N., Izquierdo, Angel, Jakubowska, Anna, James, Paul, Janavicius, Ramunas, John, Esther M., Vijai, Joseph, Karlan, Beth Y., Kast, Karin, Investigators, KConFab, Korach, Jacob, Laitman, Yael, Lasset, Christine, Lázaro, Conxi, Lee, Annette, Lee, Min Hyuk, Lester, Jenny, Liljegren, Annelie, Machackova, Eva, Mari, Véronique, Meijers‐Heijboer, Hanne E.J., Miller, Austin, Montagna, Marco, Mulligan, Anna Marie, Ngeow, Joanne, Nielsen, Henriette Roed, Nussbaum, Robert L., Offit, Kenneth, Öfverholm, Anna, Osorio, Ana, Papp, Janos, Pedersen, Inge Sokilde, Peruga, Nina, Peterlongo, Paolo, Radice, Paolo, Robson, Mark, Rodriguez, Gustavo C., Rudaitis, Vilius, Schmidt, Ane Y., Senter, Leigha, Singer, Christian F., Skytte, Anne‐Bine, Sobol, Hagay, Teixeira, Manuel R., Tischkowitz, Marc, Toland, Amanda Ewart, Topka, Sabine, Trainer, Alison H, Varesco, Liliana, Varon‐Mateeva, Raymonda, Vega, Ana, Wachenfeldt, Anna, Wang‐Gohrke, Shan, Weber, Bernhard H. F., Yannoukakos, Drakoulis, Zorn, Kristin K., Chenevix‐Trench, Georgia, Spurdle, Amanda B., Nathanson, Katherine L.

    Veröffentlicht in Human mutation

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    The FANCM:p.Arg658 truncating variant is associated with risk of triple-negative breast cancer von Catucci, Irene, Caleca, Laura, Lasheras, Sandra Viz, Kiiski, Johanna I., Michailidou, Kyriaki, Bolla, Manjeet K., Cadoo, Karen, Arnold, Norbert, Aronson, Kristan J., Auvinen, Päivi, Barrowdale, Daniel, Barwell, Julian, Beane Freeman, Laura E., Behrens, Sabine, Blanco, Amie M., Blomqvist, Carl, Bojesen, Anders, Bojesen, Stig E., Bonanni, Bernardo, Buys, Saundra S., Caligo, Maria A., Castelao, Jose E., Chang-Claude, Jenny, Clarke, Christine L., Cybulski, Cezary, de la Hoya, Miguel, Dite, Gillian S., dos-Santos-Silva, Isabel, Eccles, Diana M., Eriksson, Mikael, Evans, D. Gareth, Figueroa, Jonine, Flyger, Henrik, Friebel, Tara M., Gago-Dominguez, Manuela, Garber, Judy, García-Closas, Montserrat, Gayther, Simon A., Giles, Graham G., Goldberg, Mark S., Guénel, Pascal, Gutierrez-Barrera, Angelica M., Haiman, Christopher A., Heyworth, Jane, Hollestelle, Antoinette, Howell, Anthony, Hu, Chunling, Jakimovska, Milena, James, Paul, John, Esther M., Jung, Audrey, Lambrechts, Diether, Lubinski, Jan, Manoochehri, Mehdi, Manoukian, Siranoush, Margolin, Sara, Maurer, Tabea, Mebirouk, Noura, Miller, Austin, Nathanson, Katherine L., Newman, William G., Offit, Kenneth, Olshan, Andrew F., Pocza, Timea, Rack, Brigitte, Rau-Murthy, Rohini, Rookus, Matti A., Ross, Eric A., Ruebner, Matthias, Scheuner, Maren T., Schmutzler, Rita K., Schneider, Michael, Scott, Christopher, Sharma, Priyanka, Simard, Jacques, Singer, Christian F., Thull, Darcy L., Tischkowitz, Marc, Torres, Diana, Troester, Melissa A., Truong, Thérèse, Untch, Michael, Vachon, Celine M., van Veen, Elke M., Vega, Ana, Viel, Alessandra, Wieme, Greet, Ziogas, Argyrios, McGuffog, Lesley, Pharoah, Paul D. P., Fostira, Florentia, Andrulis, Irene L., Ramus, Susan J., Greene, Mark H., Milne, Roger L., Chenevix-Trench, Georgia, Dörk, Thilo, Schmidt, Marjanka K., Easton, Douglas F., Couch, Fergus J.

    Veröffentlicht in NPJ BREAST CANCER

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