检索结果 - Perrier, Renée

Late presentation of cancer in compound heterozygote PMS2 mutation carrier 由 van Galen, Paulien P, Perrier, Renee, Bernier, Francois P

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An unusual tumor spectrum in Lynch syndrome caused by MSH6 mutation 由 Perrier, Renee L, Van Galen, Paulein, Pasieka, Janice L, Magliocco, Tony, Innes, A Micheil

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Birt-Hogg-Dubé syndrome: a large single family cohort 由 Skolnik, Kate, Tsai, Willis H., Dornan, Kimberly, Perrier, Renée, Burrowes, Paul W., Davidson, Warren J.

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Molecular analysis distinguishes metastatic disease from second cancers in patients with retinoblastoma 由 Racher, Hilary, Soliman, Sameh, Argiropoulos, Bob, Chan, Helen S.L., Gallie, Brenda L., Perrier, Renée, Matevski, Donco, Rushlow, Diane, Piovesan, Beata, Shaikh, Furqan, MacDonald, Heather, Corson, Timothy W.

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Evolution of genetic assessment for BRCA-associated gynaecologic malignancies: a Canadian multisociety roadmap 由 McCuaig, Jeanna M, Stockley, Tracy L, Shaw, Patricia, Fung-Kee-Fung, Michael, Altman, Alon D, Bentley, James, Bernardini, Marcus Q, Cormier, Beatrice, Hirte, Hal, Kieser, Katharina, MacMillan, Andree, Meschino, Wendy S, Panabaker, Karen, Perrier, Renee, Provencher, Diane, Schrader, Kasmintan A, Serfas, Kimberly, Tomiak, Eva, Wong, Nora, Young, Sean S, Gotlieb, Walter Henri, Hoskins, Paul, Kim, Raymond H

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Cancer risks for relatives of patients with serrated polyposis 由 Win, Aung Ko, Walters, Rhiannon J., Buchanan, Daniel D., Jenkins, Mark A., Sweet, Kevin, Frankel, Wendy L., de la Chapelle, Albert, McKeone, Diane M., Walsh, Michael D., Clendenning, Mark, Pearson, Sally-Ann, Pavluk, Erika, Nagler, Belinda, Hopper, John L., Gattas, Michael R., Goldblatt, Jack, George, Jill, Suthers, Graeme K., Phillips, Kerry D., Woodall, Sonja, Arnold, Julie, Tucker, Kathy, Field, Michael, Greening, Sian, Gallinger, Steve, Aronson, Melyssa, Perrier, Renee, Woods, Michael O., Green, Jane S., Walker, Neal, Rosty, Christophe, Parry, Susan, Young, Joanne P.

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Risk Factors for Colorectal Cancer in Patients with Multiple Serrated Polyps: A Cross-Sectional Case Series from Genetics Clinics 由 Buchanan, Daniel D., Sweet, Kevin, Drini, Musa, Jenkins, Mark A., Win, Aung Ko, English, Dallas R., Walsh, Michael D., Clendenning, Mark, McKeone, Diane M., Walters, Rhiannon J., Roberts, Aedan, Pearson, Sally-Ann, Pavluk, Erika, Hopper, John L., Gattas, Michael R., Goldblatt, Jack, George, Jill, Suthers, Graeme K., Phillips, Kerry D., Woodall, Sonja, Arnold, Julie, Tucker, Kathy, Muir, Amanda, Field, Michael, Greening, Sian, Gallinger, Steven, Perrier, Renee, Baron, John A., Potter, John D., Haile, Robert, Frankel, Wendy, de la Chapelle, Albert, Macrae, Finlay, Rosty, Christophe, Walker, Neal I., Parry, Susan, Young, Joanne P.

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Performance of the McGill Interactive Pediatric OncoGenetic Guidelines for Identifying Cancer Predisposition Syndromes 由 Goudie, Catherine, Witkowski, Leora, Cullinan, Noelle, Reichman, Lara, Schiller, Ian, Tachdjian, Melissa, Armstrong, Linlea, Blood, Katherine A., Brossard, Josée, Brunga, Ledia, Cacciotti, Chantel, Caswell, Kimberly, Cellot, Sonia, Clark, Mary Egan, Clinton, Catherine, Coltin, Hallie, Felton, Kathleen, Fernandez, Conrad V., Fleming, Adam J., Fuentes-Bolanos, Noemi, Gibson, Paul, Grant, Ronald, Hammad, Rawan, Harrison, Lynn W., Irwin, Meredith S., Johnston, Donna L., Kane, Sarah, Lafay-Cousin, Lucie, Lara-Corrales, Irene, Larouche, Valerie, Mathews, Natalie, Meyn, M. Stephen, Michaeli, Orli, Perrier, Renée, Pike, Meghan, Punnett, Angela, Ramaswamy, Vijay, Say, Jemma, Somers, Gino, Tabori, Uri, Thibodeau, My Linh, Toupin, Annie-Kim, Tucker, Katherine M., van Engelen, Kalene, Vairy, Stephanie, Waespe, Nicolas, Warby, Meera, Wasserman, Jonathan D., Whitlock, James A., Sinnett, Daniel, Jabado, Nada, Nathan, Paul C., Shlien, Adam, Kamihara, Junne, Deyell, Rebecca J., Ziegler, David S., Nichols, Kim E., Dendukuri, Nandini, Malkin, David, Villani, Anita, Foulkes, William D.

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