Zobrazeno 1 - 2
of 2
pro vyhledávání: '"van Roozendaal, Cees E."'
Autor:
Im, Kate M., Kirchhoff, Tomas, Wang, Xianshu, Green, Todd, Chow, Clement Y., Vijai, Joseph, Korn, Joshua, Gaudet, Mia M., Fredericksen, Zachary, Pankratz, V. Shane, Guiducci, Candace, Crenshaw, Andrew, McGuffog, Lesley, Kartsonaki, Christiana, Morrison, Jonathan, Healey, Sue, Sinilnikova, Olga M., Mai, Phuong L., Greene, Mark H., Piedmonte, Marion, Rubinstein, Wendy S., Hogervorst, Frans B. L., Rookus, Matti A., Collee, Margriet J., Hoogerbrugge, Nicoline, van Asperen, Christi J., Meijers-Heijboer, Hanne E. J., van Roozendaal, Cees E., Caldes, Trinidad, Perez Segura, Pedro, Jakubowska, Anna, Lubinski, Jan, Huzarski, Tomasz, Blecharz, Pawel, Nevanlinna, Heli, Aittomaki, Kristiina, Lazaro, Conxi, Blanco, Ignacio, Barkardottir, Rosa B., Montagna, Marco, D'Andrea, Emma, Devilee, Peter, Olopade, Olufunmilayo I., Neuhausen, Susan L., Peissel, Bernard, Bonanni, Bernardo, Peterlongo, Paolo, Singer, Christian F., Rennert, Gad, Lejbkowicz, Flavio, Andrulis, Irene L., Glendon, Gord, Ozcelik, Hilmi, Toland, Amanda Ewart, Caligo, Maria Adelaide, Beattie, Mary S., Chan, Salina B., Domchek, Susan M., Nathanson, Katherine L., Rebbeck, Timothy R., Phelan, Catherine M., Narod, Steven A., John, Esther M., Hopper, John L., Buys, Saundra, Daly, Mary B., Southey, Melissa C., Terry, Mary Beth, Tung, Nadine, Hansen, Thomas V. O., Osorio, Ana, Benitez, Javier, Duran, Mercedes, Weitzel, Jeffrey N., Garber, Judy, Hamann, Ute, Peock, Susan, Cook, Margaret, Oliver, Clare T., Frost, Debra, Platte, Radka, Evans, D. Gareth, Eeles, Ros, Izatt, Louise, Paterson, Joan, Brewer, Carole, Hodgson, Shirley V., Morrison, Patrick J., Porteous, Mary E., Walker, Lisa, Rogers, Mark T., Side, Lucy E., Godwin, Andrew K., Schmutzler, Rita K., Wappenschmidt, Barbara, Laitman, Yael, Meindl, Alfons, Deissler, Helmut, Varon-Mateeva, Raymonda, Preisler-Adams, Sabine, Kast, Karin, Venat-Bouvet, Laurence, Stoppa-Lyonnet, Dominique, Chenevix-Trench, Georgia, Easton, Douglas F., Klein, Robert J., Daly, Mark J., Friedman, Eitan, Dean, Michael, Clark, Andrew G., Altshuler, David M., Antoniou, Antonis C., Couch, Fergus J., Offit, Kenneth, Gomez Garcia, Encarna, Blok, Marinus, Gold, Bert
Publikováno v:
Human Genetics
Human Genetics, Springer Verlag, 2011, 130 (5), pp.685-99. 〈10.1007/s00439-011-1003-z〉
Human Genetics, Springer Verlag, 2011, 130 (5), pp.685-99. ⟨10.1007/s00439-011-1003-z⟩
Human Genetics, 130(5), 685-699. Springer
Im, K M, Kirchhoff, T, Wang, X S, Green, T, Chow, C Y, Vijai, J, Korn, J, Gaudet, M M, Fredericksen, Z, Pankratz, V S, Guiducci, C, Crenshaw, A, McGuffog, L, Kartsonaki, C, Morrison, J, Healey, S, Sinilnikova, O M, Mai, P L, Greene, M H, Piedmonte, M, Rubinstein, W S, Hogervorst, FB, Rookus, M A, Collee, J M, Hoogerbrugge, N, van Asperen, C J, Meijers-Heijboer, E J, van Roozendaal, C E, Caldes, T, Perez-Segura, P, Jakubowska, A, Lubinski, J, Huzarski, T, Blecharz, P, Nevanlinna, H, Aittomaki, K, Lazaro, C, Blanco, I, Barkardottir, R B, Montagna, M, D'Andrea, E, Devilee, P, Olopade, O I, Neuhausen, S L, Peissel, B, Bonanni, B, Peterlongo, P, Singer, C F, Rennert, G, Lejbkowicz, F, Andrulis, I L, Glendon, G, Ozcelik, H, Toland, A E, Caligo, M A, Beattie, M S, Chan, S, Domchek, S M, Nathanson, K L, Rebbeck, T R, Phelan, C, Narod, S, John, E M, Hopper, J L, Buys, S S, Daly, M B, Southey, M C, Terry, M B, Tung, N, Hansen, T V O, Osorio, A, Benitez, J, Duran, M, Weitzel, J N, Garber, J, Hamann, U, Peock, S, Cook, M, Oliver, C T, Frost, D, Platte, R, Evans, D G, Eeles, R, Izatt, L, Paterson, J, Brewer, C, Hodgson, S, Morrison, P J, Porteous, M, Walker, L, Rogers, M T, Side, L E, Godwin, A K, Schmutzler, R K, Wappenschmidt, B, Laitman, Y, Meindl, A, Deissler, H & Varon-Mateeva, R 2011, ' Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers ', Human Genetics, vol. 130, no. 5, pp. 685-699 . https://doi.org/10.1007/s00439-011-1003-z
Human Genetics, 130, 685-99
Human genetics, 130(5), 685-699. Springer Verlag
Recercat. Dipósit de la Recerca de Catalunya
instname
Digital.CSIC. Repositorio Institucional del CSIC
Human Genetics, 130(5), 685-699. Springer-Verlag
Dipòsit Digital de la UB
Universidad de Barcelona
Human Genetics, 130(5), 685-699
Human Genetics, 130(5), 685-699. Springer Verlag
Human Genetics, 130, 5, pp. 685-99
Human Genetics, Springer Verlag, 2011, 130 (5), pp.685-99. 〈10.1007/s00439-011-1003-z〉
Human Genetics, Springer Verlag, 2011, 130 (5), pp.685-99. ⟨10.1007/s00439-011-1003-z⟩
Human Genetics, 130(5), 685-699. Springer
Im, K M, Kirchhoff, T, Wang, X S, Green, T, Chow, C Y, Vijai, J, Korn, J, Gaudet, M M, Fredericksen, Z, Pankratz, V S, Guiducci, C, Crenshaw, A, McGuffog, L, Kartsonaki, C, Morrison, J, Healey, S, Sinilnikova, O M, Mai, P L, Greene, M H, Piedmonte, M, Rubinstein, W S, Hogervorst, FB, Rookus, M A, Collee, J M, Hoogerbrugge, N, van Asperen, C J, Meijers-Heijboer, E J, van Roozendaal, C E, Caldes, T, Perez-Segura, P, Jakubowska, A, Lubinski, J, Huzarski, T, Blecharz, P, Nevanlinna, H, Aittomaki, K, Lazaro, C, Blanco, I, Barkardottir, R B, Montagna, M, D'Andrea, E, Devilee, P, Olopade, O I, Neuhausen, S L, Peissel, B, Bonanni, B, Peterlongo, P, Singer, C F, Rennert, G, Lejbkowicz, F, Andrulis, I L, Glendon, G, Ozcelik, H, Toland, A E, Caligo, M A, Beattie, M S, Chan, S, Domchek, S M, Nathanson, K L, Rebbeck, T R, Phelan, C, Narod, S, John, E M, Hopper, J L, Buys, S S, Daly, M B, Southey, M C, Terry, M B, Tung, N, Hansen, T V O, Osorio, A, Benitez, J, Duran, M, Weitzel, J N, Garber, J, Hamann, U, Peock, S, Cook, M, Oliver, C T, Frost, D, Platte, R, Evans, D G, Eeles, R, Izatt, L, Paterson, J, Brewer, C, Hodgson, S, Morrison, P J, Porteous, M, Walker, L, Rogers, M T, Side, L E, Godwin, A K, Schmutzler, R K, Wappenschmidt, B, Laitman, Y, Meindl, A, Deissler, H & Varon-Mateeva, R 2011, ' Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers ', Human Genetics, vol. 130, no. 5, pp. 685-699 . https://doi.org/10.1007/s00439-011-1003-z
Human Genetics, 130, 685-99
Human genetics, 130(5), 685-699. Springer Verlag
Recercat. Dipósit de la Recerca de Catalunya
instname
Digital.CSIC. Repositorio Institucional del CSIC
Human Genetics, 130(5), 685-699. Springer-Verlag
Dipòsit Digital de la UB
Universidad de Barcelona
Human Genetics, 130(5), 685-699
Human Genetics, 130(5), 685-699. Springer Verlag
Human Genetics, 130, 5, pp. 685-99
Three founder mutations in BRCA1 and BRCA2 contribute to the risk of hereditary breast and ovarian cancer in Ashkenazi Jews (AJ). They are observed at increased frequency in the AJ compared to other BRCA mutations in Caucasian non-Jews (CNJ). Several
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b76209a3052a1556a0f6f989a4c88d4
https://hal.archives-ouvertes.fr/hal-00837832
https://hal.archives-ouvertes.fr/hal-00837832
Autor:
Im KM; Center for Cancer Research, Cancer Inflammation Program, Human Genetics Section, National Cancer Institute, Frederick, MD, USA., Kirchhoff T, Wang X, Green T, Chow CY, Vijai J, Korn J, Gaudet MM, Fredericksen Z, Shane Pankratz V, Guiducci C, Crenshaw A, McGuffog L, Kartsonaki C, Morrison J, Healey S, Sinilnikova OM, Mai PL, Greene MH, Piedmonte M, Rubinstein WS, Hogervorst FB, Rookus MA, Collée JM, Hoogerbrugge N, van Asperen CJ, Meijers-Heijboer HE, Van Roozendaal CE, Caldes T, Perez-Segura P, Jakubowska A, Lubinski J, Huzarski T, Blecharz P, Nevanlinna H, Aittomäki K, Lazaro C, Blanco I, Barkardottir RB, Montagna M, D'Andrea E, Devilee P, Olopade OI, Neuhausen SL, Peissel B, Bonanni B, Peterlongo P, Singer CF, Rennert G, Lejbkowicz F, Andrulis IL, Glendon G, Ozcelik H, Toland AE, Caligo MA, Beattie MS, Chan S, Domchek SM, Nathanson KL, Rebbeck TR, Phelan C, Narod S, John EM, Hopper JL, Buys SS, Daly MB, Southey MC, Terry MB, Tung N, Hansen TV, Osorio A, Benitez J, Durán M, Weitzel JN, Garber J, Hamann U, Peock S, Cook M, Oliver CT, Frost D, Platte R, Evans DG, Eeles R, Izatt L, Paterson J, Brewer C, Hodgson S, Morrison PJ, Porteous M, Walker L, Rogers MT, Side LE, Godwin AK, Schmutzler RK, Wappenschmidt B, Laitman Y, Meindl A, Deissler H, Varon-Mateeva R, Preisler-Adams S, Kast K, Venat-Bouvet L, Stoppa-Lyonnet D, Chenevix-Trench G, Easton DF, Klein RJ, Daly MJ, Friedman E, Dean M, Clark AG, Altshuler DM, Antoniou AC, Couch FJ, Offit K, Gold B
Publikováno v:
Human genetics [Hum Genet] 2011 Nov; Vol. 130 (5), pp. 685-99. Date of Electronic Publication: 2011 May 20.