Measurement of negatively charged pion spectra in inelastic p+p interactions at ... 20, 31, 40, 80 and 158 GeV/c: NA61/SHINE Collaboration by Abgrall, N, Aduszkiewicz, A, Ali, Y, Anticic, T, Antoniou, N, Baatar, B, Bay, F, Blondel, A, Blumer, J, Bogomilov, M, Bravar, A, Brzychczyk, J, Bunyatov, SA, Busygina, O, Christakoglou, P, Czopowicz, T, Davis, N, Debieux, S, Dembinski, H, Diakonos, F, Luise, SDi, Dominik, W, Drozhzhova, T, Dumarchez, J, Dynowski, K, Engel, R, Ereditato, A, Feofilov, G A, Fodor, Z, Fulop, A, Gadzicki, M, Golubeva, M, Grebieszkow, K, Grzeszczuk, A, Guber, F, Haesler, A, Hasegawa, T, Hierholzer, M, Idczak, R, Igolkin, S, Ivashkin, A, Jokovic, D, Kadija, K, Kapoyannis, A, Kaptur, E, Kieczewska, D, Kirejczyk, M, Kisiel, J, Kiss, T, Kleinfelder, S, et. al

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Ω, J/ψ and ψ′ transverse mass spectra at RHIC by Bugaev, K.A, Gaździcki, M, Gorenstein, M.I

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Expanding the phenotype of a recurrent de novo variant in PACS1 causing intellectual disability by Gadzicki, D., Döcker, D., Schubach, M., Menzel, M., Schmorl, B., Stellmer, F., Biskup, S., Bartholdi, D.

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Search for deconfinement in NA49 at the CERN SPS by Seyboth, Peter, Afanasiev, S. V., Anticic, T., Barna, D., Bartke, J., Barton, R. A., Betev, L., Bialkowska, H., Billmeier, A., Blume, C., Blyth, C. O., Boimska, B., Botje, M., Bracinik, J., Bramm, R., Brun, R., Bunci, P., Cerny, V., Chvala, O., Cramer, J. G., Csato, P., Dinkelaker, P., Eckardt, V., Filip, P., Fischer, H. G., Fodor, Z., Foka, P., Freund, P., Friese, V., Gal, J., Gaździcki, M., Georgopoulos, G., Gladysz, E., Hegyi, S., Hohne, C., Jones, P. G., Kadija, K., Karev, A., Kolesnikov, V. I., Kollegger, T., Kowalski, M., Kraus, I., Kreps, M., van Leeuwen, M., Levai, P., Malakhov, A. I., Markert, C., WMayes, B., Melkumov, G. L., Mischke, A., Molnar, J., Nelson, J. M., Palla, G., Panagiotou, A. D., Perl, K., Petridis, A., Pikna, M., Pinsky, L., Puhlhofer, F., Reid, J. G., Renfordt, R., Retyk, W., Roland, C., Roland, G., Rybicki, A., Sandoval, A., Sann, H., Schmitz, N., Sikler, F., Sitar, B., Skrzypczak, E., Squier, G. T. A., Stock, R., Strobele, H., Susa, T., Szentpetery, I., Sziklai, J., Trainor, T. A., Varga, D., Vassiliou, M., Veres, G. I., Vesztergombi, G., Vranic, D., Wenig, S., Wetzler, A., KYoo, I., Zaranek, J., Zimanyi, J.

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Pathology of Breast and Ovarian Cancers among BRCA1 and BRCA2 Mutation Carriers: Results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA) by MAVADDAT, Nasim, BARROWDALE, Daniel, MULLIGAN, Anna Marie, COUCH, Fergus J, ENGEL, Christoph, MCGUFFOG, Lesley, HEALER, Sue, SINILNIKOVA, Olga M, SOUTHEY, Melissa C, TERRY, Mary Beth, GOLDGAR, David, O'MALLEY, Frances, ANDRULIS, Irene L, JOHN, Esther M, JANAVICIUS, Ramunas, TIHOMIROVA, Laima, HANSEN, Thomas V. O, NIELSEN, Finn C, OSORIO, Ana, STAVROPOULOU, Alexandra, BENITEZ, Javier, MANOUKIAN, Siranoush, PEISSEL, Bernard, DOMCHEK, Susan M, BARILE, Monica, VOLORIO, Sara, PASIN, Barbara, DOLCETTI, Riccardo, PUTIGNANO, Anna Laura, OTTINI, Laura, RADICE, Paolo, HAMANN, Ute, RASHID, Muhammad U, HOGERVORST, Frans B, ECCLES, Diana, KRIEGE, Mieke, VAN DER LUIJT, Rob B, HEBON, PEOCK, Susan, FROST, Debra, GARETH EVANS, D, BREWER, Carole, WALKER, Lisa, ROGERS, Mark T, SIDE, Lucy E, NEVANLINNA, Heli, HOUGHTON, Catherine, EMBRACE, WEAVER, Joellen, GODWIN, Andrew K, SCHMUTZLER, Rita K, WAPPENSCHMIDT, Barbara, MEINDL, Alfons, KAST, Karin, RAMUS, Susan J, SPURDLE, Amanda, ROBSON, Mark, SHERMAN, Mark

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Clinical delineation of the PACS1-related syndrome-Report on 19 patients by Schuurs-Hoeijmakers, Janneke H. M., Landsverk, Megan L., Foulds, Nicola, Kukolich, Mary K., Gavrilova, Ralitza H., Greville-Heygate, Stephanie, Hanson-Kahn, Andrea, Bernstein, Jonathan A., Glass, Jennifer, Chitayat, David, Burrow, Thomas A., Husami, Ammar, Collins, Kathleen, Wusik, Katie, van der Aa, Nathalie, Kooy, Frank, Brown, Kate Tatton, Gadzicki, Dorothea, Kini, Usha, Alvarez, Sara, Fernández-Jaén, Alberto, McGehee, Frank, Selby, Katherine, Tarailo-Graovac, Maja, Van Allen, Margot, van Karnebeek, Clara D. M., Stavropoulos, Dimitri J., Marshall, Christian R., Merico, Daniele, Gregor, Anne, Zweier, Christiane, Hopkin, Robert J., Chu, Yoyo Wing-Yiu, Chung, Brian Hon-Yin, de Vries, Bert B. A., Devriendt, Koenraad, Hurles, Matthew E., Brunner, Han G.

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An evaluation of the polymorphisms Ins16bp and Arg72Pro in p53 as breast cancer risk modifiers in BRCA1 and BRCA2 mutation carriers by Osorio, A, Pollán, M, Pita, G, Schmutzler, R K, Versmold, B, Engel, C, Meindl, A, Arnold, N, Preisler-Adams, S, Niederacher, D, Hofmann, W, Gadzicki, D, Jakubowska, A, Hamann, U, Lubinski, J, Toloczko-Grabarek, A, Cybulski, C, Debniak, T, Llort, G, Yannoukakos, D, Díez, O, Peissel, B, Peterlongo, P, Radice, P, Heikkinen, T, Nevanlinna, H, Mai, P L, Loud, J T, McGuffog, L, Antoniou, A C, Benitez, J

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Tourette syndrome is not caused by mutations in the central cannabinoid receptor (CNR1) gene by Gadzicki, Dorothea, Müller-Vahl, Kirsten R., Heller, Daniela, Ossege, Sebastian, Nöthen, Markus M., Hebebrand, Johannes, Stuhrmann, Manfred

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A frequent polymorphism in the coding exon of the human cannabinoid receptor (CNR1) gene by Gadzicki, D, Müller-Vahl, K, Stuhrmann, M

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Jacobsen Syndrome and Beckwith‐Wiedemann Syndrome Caused by a Parental Pericentric Inversion inv(11)(p15q24) by Gadzicki, D., Baumer, A., Wey, E., Happel, C. M., Rudolph, C., Tönnies, H., Neitzel, H., Steinemann, D., Welte, K., Klein, C., Schlegelberger, B.

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Impact of BRCA mutation status on the clinical phenotype and survival of hereditary breast cancer by Kiechle, M, Engel, C, Schwarz-Boeger, U, Grund, D, Preisler-Adams, S, Crohns, C, Stark, S, Gadzicki, D, Strunz, K, Schoenbuchner, I, Nestle-Kräemeling, C, Kast, K, Ditsch, N, Schlehe, B, Schmutzler, R

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Correction: Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer by Kirchhoff, Tomas, Green, Todd, Vijai, Joseph, Korn, Joshua M., Guiducci, Candace, Segrè, Ayellet V., McGee, Kate, McGuffog, Lesley, Healey, Sue, Sinilnikova, Olga M., Stoppa-Lyonnet, Dominique, Gauthier-Villars, Marion, Sobol, Hagay, Longy, Michel, GEMO Study Collaborators, Frans B. L., Rookus, Matti A., Hoogerbrugge, Nicoline, van Roozendaal, Kees E. P., Piedmonte, Marion, Rubinstein, Wendy, Nerenstone, Stacy, Van Le, Linda, Blank, Stephanie V., Caldés, Trinidad, Nevanlinna, Heli, Lazaro, Conxi, Blanco, Ignacio, Arason, Adalgeir, Johannsson, Oskar T., Barkardottir, Rosa B., Devilee, Peter, Olopade, Olofunmilayo I., Neuhausen, Susan L., Wang, Xianshu, Fredericksen, Zachary S., Peterlongo, Paolo, Manoukian, Siranoush, Viel, Alessandra, Radice, Paolo, Phelan, Catherine M., Narod, Steven, Rennert, Gad, Lejbkowicz, Flavio, Flugelman, Anath, Andrulis, Irene L., Glendon, Gord, Ozcelik, Hilmi, Toland, Amanda E., D'Andrea, Emma, Friedman, Eitan, Borg, Ake, Beattie, Mary, Ramus, Susan J., Domchek, Susan M., Nathanson, Katherine L., Rebbeck, Tim, Spurdle, Amanda B., Chen, Xiaoqing, Holland, Helene, John, Esther M., Hopper, John L., Buys, Saundra S., Southey, Melissa C., Terry, Mary Beth, Tung, Nadine, Overeem Hansen, Thomas V., Nielsen, Finn C., Greene, Mark H., Mai, Phuong L., Osorio, Ana, Durán, Mercedes, Andres, Raquel, Benítez, Javier, Weitzel, Jeffrey N., Hamann, Ute, Cook, Margaret, Oliver, Clare, Frost, Debra, Platte, Radka, Evans, D. Gareth, Eeles, Ros, Izatt, Louise, Walker, Lisa, Eason, Jacqueline, Barwell, Julian, Godwin, Andrew K., Schmutzler, Rita K., Wappenschmidt, Barbara, Engert, Stefanie, Arnold, Norbert, Gadzicki, Dorothea, Dean, Michael, Gold, Bert, Klein, Robert J., Couch, Fergus J., Chenevix-Trench, Georgia, Daly, Mark J., Antoniou, Antonis C., Altshuler, David M., Offit, Kenneth

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Correction: Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer by Kirchhoff, Tomas, Green, Todd, Vijai, Joseph, Korn, Joshua M, Guiducci, Candace, McGee, Kate, McGuffog, Lesley, Healey, Sue, Stoppa-Lyonnet, Dominique, Gauthier-Villars, Marion, Sobol, Hagay, Longy, Michel, GEMO Study Collaborators, Hogervorst, Frans BL, Collee, JMargriet, Hoogerbrugge, Nicoline, van Roozendaal, Kees EP, Piedmonte, Marion, Rubinstein, Wendy, Nerenstone, Stacy, Van Le, Linda, Blank, Stephanie V, Caldes, Trinidad, de la Hoya, Miguel, Nevanlinna, Heli, Aittomaeki, Kristiina, Blanco, Ignacio, Arason, Adalgeir, Johannsson, Oskar T, Barkardottir, Rosa B, Devilee, Peter, Olopade, Olofunmilayo I, Neuhausen, Susan L, Wang, Xianshu, Fredericksen, Zachary S, Manoukian, Siranoush, Barile, Monica, Viel, Alessandra, Radice, Paolo, Phelan, Catherine M, Narod, Steven, Lejbkowicz, Flavio, Flugelman, Anath, Andrulis, Irene L, Glendon, Gord, Ozcelik, Hilmi, Toland, Amanda E, Montagna, Marco, D'Andrea, Emma, Laitman, Yael, Ramus, Susan J, Domchek, Susan M, Nathanson, Katherine L, Rebbeck, Tim, Spurdle, Amanda B, Chen, Xiaoqing, Holland, Helene, John, Esther M, Hopper, John L, Buys, Saundra S, Daly, Mary B, Southey, Melissa C, Terry, Mary Beth, Tung, Nadine, Nielsen, Finn C, Greene, Mark I, Mai, Phuong L, Duran, Mercedes, Andres, Raquel, Benitez, Javier, Weitzel, Jeffrey N, Garber, Judy, Hamann, Ute, Peock, Susan, Cook, Margaret, Oliver, Clare, Frost, Debra, Platte, Radka, Evans, DGareth, Lalloo, Fiona, Eeles, Ros, Izatt, Louise, Walker, Lisa, Eason, Jacqueline, Barwell, Julian, Godwin, Andrew K, Schmutzler, Rita K, Wappenschmidt, Barbara, Engert, Stefanie, Arnold, Norbert, Gadzicki, Dorothea, Dean, Michael, Gold, Bert, Klein, Robert J, Couch, Fergus J, Chenevix-Trench, Georgia, Easton, Douglas F, Antoniou, Antonis C, Altshuler, David M, Offit, Kenneth

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Correction: Common Genetic Variants and Modification of Penetrance of -Associated Breast Cancer by Tomas Kirchhoff, Todd Green, Joseph Vijai, Joshua M. Korn, Candace Guiducci, Ayellet V. Segrè, Kate McGee, Lesley McGuffog, Christiana Kartsonaki, Jonathan Morrison, Olga M. Sinilnikova, Dominique Stoppa-Lyonnet, Sylvie Mazoyer, Marion Gauthier-Villars, Hagay Sobol, Michel Longy, Marc Frenay, GEMO Study Collaborators, Frans B. L. Hogervorst, J. Margriet Collée, Nicoline Hoogerbrugge, Kees E. P. van Roozendaal, Marion Piedmonte, Wendy Rubinstein, Stacy Nerenstone, Linda Van Le, Stephanie V. Blank, Trinidad Caldés, Heli Nevanlinna, Kristiina Aittomäki, Conxi Lazaro, Ignacio Blanco, Adalgeir Arason, Oskar T. Johannsson, Rosa B. Barkardottir, Peter Devilee, Susan L. Neuhausen, Xianshu Wang, Zachary S. Fredericksen, Paolo Peterlongo, Siranoush Manoukian, Monica Barile, Alessandra Viel, Paolo Radice, Gad Rennert, Anath Flugelman, Irene L. Andrulis, Gord Glendon, Hilmi Ozcelik, Amanda E. Toland, Emma D'Andrea, Eitan Friedman, Yael Laitman, Mary Beattie, Susan J. Ramus, Susan M. Domchek, Katherine L. Nathanson, Tim Rebbeck, Amanda B. Spurdle, Xiaoqing Chen, Helene Holland, Esther M. John, Melissa C. Southey, Mary Beth Terry, Nadine Tung, Thomas V. Overeem Hansen, Finn C. Nielsen, Mark I. Greene, Phuong L. Mai, Ana Osorio, Mercedes Durán, Javier Benítez, Jeffrey N. Weitzel, Judy Garber, Ute Hamann, Susan Peock, Margaret Cook, Clare Oliver, Debra Frost, Radka Platte, D. Gareth Evans, Fiona Lalloo, Louise Izatt, Lisa Walker, Jacqueline Eason, Julian Barwell, Andrew K. Godwin, Rita K. Schmutzler, Barbara Wappenschmidt, Stefanie Engert, Norbert Arnold, Dorothea Gadzicki, Michael Dean, Bert Gold, Robert J. Klein, Fergus J. Couch, Georgia Chenevix-Trench, Douglas F. Easton, David M. Altshuler, Kenneth Offit

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Correction: Common Genetic Variants and Modification of Penetrance of -Associated Breast Cancer by Tomas Kirchhoff, Todd Green, Joseph Vijai, Joshua M. Korn, Candace Guiducci, Ayellet V. Segrè, Kate McGee, Lesley McGuffog, Christiana Kartsonaki, Jonathan Morrison, Olga M. Sinilnikova, Dominique Stoppa-Lyonnet, Sylvie Mazoyer, Marion Gauthier-Villars, Hagay Sobol, Michel Longy, Marc Frenay, GEMO Study Collaborators, Frans B. L. Hogervorst, J. Margriet Collée, Nicoline Hoogerbrugge, Kees E. P. van Roozendaal, Marion Piedmonte, Wendy Rubinstein, Stacy Nerenstone, Linda Van Le, Stephanie V. Blank, Trinidad Caldés, Heli Nevanlinna, Kristiina Aittomäki, Conxi Lazaro, Ignacio Blanco, Adalgeir Arason, Oskar T. Johannsson, Rosa B. Barkardottir, Peter Devilee, Susan L. Neuhausen, Xianshu Wang, Zachary S. Fredericksen, Paolo Peterlongo, Siranoush Manoukian, Monica Barile, Alessandra Viel, Paolo Radice, Gad Rennert, Anath Flugelman, Irene L. Andrulis, Gord Glendon, Hilmi Ozcelik, Amanda E. Toland, Emma D'Andrea, Eitan Friedman, Yael Laitman, Mary Beattie, Susan J. Ramus, Susan M. Domchek, Katherine L. Nathanson, Tim Rebbeck, Amanda B. Spurdle, Xiaoqing Chen, Helene Holland, Esther M. John, Melissa C. Southey, Mary Beth Terry, Nadine Tung, Thomas V. Overeem Hansen, Finn C. Nielsen, Mark H. Greene, Phuong L. Mai, Ana Osorio, Mercedes Durán, Javier Benítez, Jeffrey N. Weitzel, Judy Garber, Ute Hamann, Susan Peock, Margaret Cook, Clare Oliver, Debra Frost, Radka Platte, D. Gareth Evans, Fiona Lalloo, Louise Izatt, Lisa Walker, Jacqueline Eason, Julian Barwell, Andrew K. Godwin, Rita K. Schmutzler, Barbara Wappenschmidt, Stefanie Engert, Norbert Arnold, Dorothea Gadzicki, Michael Dean, Bert Gold, Robert J. Klein, Fergus J. Couch, Georgia Chenevix-Trench, Douglas F. Easton, David M. Altshuler, Kenneth Offit

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Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2mutation carriers by Antoniou, Antonis C, Soucy, Penny, Beesley, Jonathan, McGuffog, Lesley, Lee, Andrew, Healey, Sue, Lindblom, Annika, Arver, Brita, Karlsson, Per, Nathanson, Kate, Domchek, Susan, Rebbeck, Tim, Jakubowska, Anna, Lubinski, Jan, Jaworska, Katarzyna, ZÅowowcka-PerÅowska, Elżbieta, Osorio, Ana, Andrñs, Raquel, Hamann, Ute, Verhoef, Senno, Wijnen, Juul, Gómez Garcia, Encarna B, Ligtenberg, Marjolijn J, Kriege, Mieke, Ausems, Margreet GEM, Oosterwijk, Jan C, Fineberg, Elena, Lalloo, Fiona, Davidson, Rosemarie, Cook, Jackie, Paterson, Joan, Douglas, Fiona, Brewer, Carole, Hodgson, Shirley, Morrison, Patrick J, Walker, Lisa, Rogers, Mark T, Donaldson, Alan, Dorkins, Huw, Godwin, Andrew K, Bove, Betsy, Stoppa-Lyonnet, Dominique, Houdayer, Claude, Buecher, Bruno, de Pauw, Antoine, Mazoyer, Sylvie, Bressac- de Paillerets, Brigitte, Caron, Olivier, Frenay, Marc, Ferrer, Sandra Fert, Mortemousque, Isabelle, Daly, Mary, Southey, Melissa, Goldgar, David, Kaulich, Daphne Geschwantler, Nielsen, Finn C, Barkardottir, Rosa B, Kirchhoff, Tomas, Joseph, Vijai, Piedmonte, Marion, Cohn, David, Fiorica, James, Oliani, Cristina, Tihomirova, Laima, Blanco, Ignacio, Valle, J Del, Gayther, Simon A, Teo, Soo-Hwang, Ganz, Patricia A, Beattie, Mary S, Wappenschmidt, Barbara, Ditsch, Nina, Heidemann, Simone, Preisler-Adams, Sabine, Gadzicki, Dorothea, Varon-Mateeva, Raymonda, Gehrig, Andrea, Caldes, Trinidad, Nevanlinna, Heli, Muranen, Taru A, Lespñrance, Bernard, Spurdle, Amanda B, Neuhausen, Susan L, Ding, Yuan C, Pankratz, Vernon S, Manoukian, Siranoush, Peissel, Bernard, Zaffaroni, Daniela, Papi, Laura, Ottini, Laura, Radice, Paolo, Loud, Jennifer T, Andrulis, Irene L, Ozcelik, Hilmi, Glendon, Gord, Thomassen, Mads, Kruse, Torben A, Chenevix-Trench, Georgia, Couch, Fergus J, Simard, Jacques

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An evaluation of the polymorphisms Ins 16bp and Arg72Pro in p53 as breast cancer risk modifiers in BRCA1 and BRCA2 mutation carriers by Osorio, A, Pollan, M, Pita, G, Schmutzler, R K, Versmold, B, Engel, C, Meindl, A, Arnold, N, Preisler-Adams, S, Niederacher, D, Hofmann, W, Gadzicki, D, Jakubowska, A, Hamann, U

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Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer: e1001183 by Kirchhoff, Tomas, Green, Todd, Vijai, Joseph, Korn, Joshua M, Guiducci, Candace, Segrè, Ayellet V, McGee, Kate, McGuffog, Lesley, Healey, Sue, Stoppa-Lyonnet, Dominique, Gauthier-Villars, Marion, Sobol, Hagay, Longy, Michel, Collaborators, GEMO Study, Hogervorst, Frans BL, Collée, J Margriet, Hoogerbrugge, Nicoline, Roozendaal, E Pvan, Piedmonte, Marion, Rubinstein, Wendy, Nerenstone, Stacy, Le, Linda Van, Blank, Stephanie V, Hoya, Miguel dela, Nevanlinna, Heli, Aittomäki, Kristiina, Blanco, Ignacio, Arason, Adalgeir, Johannsson, Oskar T, Barkardottir, Rosa B, Devilee, Peter, Olopade, Olofunmilayo I, Neuhausen, Susan L, Wang, Xianshu, Fredericksen, Zachary S, Manoukian, Siranoush, Barile, Monica, Viel, Alessandra, Radice, Paolo, Phelan, Catherine M, Narod, Steven, Lejbkowicz, Flavio, Flugelman, Anath, Andrulis, Irene L, Glendon, Gord, Ozcelik, Hilmi, Toland, Amanda E, Montagna, Marco, Friedman, Eitan, Borg, Ake, Beattie, Mary, Ramus, Susan J, Domchek, Susan M, Nathanson, Katherine L, Rebbeck, Tim, Spurdle, Amanda B, Chen, Xiaoqing, Holland, Helene, John, Esther M, Hopper, John L, Buys, Saundra S, Daly, Mary B, Southey, Melissa C, Terry, Mary Beth, Tung, Nadine, Hansen, Thomas VOvereem, Nielsen, Finn C, Greene, Mark I, Mai, Phuong L, Osorio, Ana, Durán, Mercedes, Andres, Raquel, Benítez, Javier, Weitzel, Jeffrey N, Hamann, Ute, Cook, Margaret, Oliver, Clare, Frost, Debra, Platte, Radka, Evans, D Gareth, Eeles, Ros, Izatt, Louise, Walker, Lisa, Eason, Jacqueline, Barwell, Julian, Godwin, Andrew K, Schmutzler, Rita K, Wappenschmidt, Barbara, Engert, Stefanie, Arnold, Norbert, Gadzicki, Dorothea, Dean, Michael, Gold, Bert, Couch, Fergus J, Chenevix-Trench, Georgia, Easton, Douglas F, Daly, Mark J, Antoniou, Antonis C, Offit, Kenneth, Collaborators, HEBON Study

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Power law in hadron production by Gaździcki, Marek, Gorenstein, Mark I.

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An evaluation of the polymorphisms Ins 16bp and Arg72Pro in p53 as breast cancer risk modifiers in BRCAI and BRCA2 mutation carriers by OSORIO, A, POLLAN, M, HOFMANN, W, GADZICKI, D, JAKUBOWSKA, A, HAMANN, U, LUBINSKI, J, TOLOCZKO-GRABAREK, A, CYBULSKI, C, DEBNIAK, T, LIORT, G, YANNOUKAKOS, D, PITA, G, DIEZ, O, PEISSEL, B, PETERLONGO, P, RADICE, P, HEIKKINEN, T, NEVANLINNA, H, MAI, P. L, LOUD, J. T, MCGUFFOG, L, ANTONIOU, A. C, SCHMUTZLER, R. K, BENITEZ, J, VERSMOLD, B, ENGEL, C, MEINDL, A, ARNOLD, N, PREISLER-ADAMS, S, NIEDERACHER, D

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