Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Fornes Claudia"'
Autor:
Dourisboure Ricardo J, Nicolorich Maria V, de La Vega Elena Carlos D, Landi Carolina, Fornes Claudia, Chialina Sergio G, Solano Angela, Solis Edita A
Publikováno v:
BMC Medical Genetics, Vol 7, Iss 1, p 5 (2006)
Abstract Background Hereditary non-polyposis colon cancer (HNPCC) is an autosomal dominant syndrome predisposing to the early development of various cancers including those of colon, rectum, endometrium, ovarium, small bowel, stomach and urinary trac
Externí odkaz:
https://doaj.org/article/2a8a6c0e2562452581ff92bc0b439463
Autor:
Chialina, Sergio G1 sergiochialina@hotmail.com, Fornes, Claudia1 fornesclaudia@hotmail.com, Landi, Carolina1 carolinalandi@hotmail.com, de La Vega Elena, Carlos D1 cddelavega@yahoo.com, Nicolorich, Maria V1 mvnicolorich@hotmail.com, Dourisboure, Ricardo J2 douris@elsitio.net, Solano, Angela2 asolano@ciudad.com.ar, Solis, Edita A1 editasolis@hotmail.com
Publikováno v:
BMC Medical Genetics. 2006, Vol. 7, p5-5. 5p. 3 Black and White Photographs, 1 Chart.
Autor:
Thompson, Bryony A, Spurdle, Amanda B, Plazzer, John-Paul, Greenblatt, Marc S, Akagi, Kiwamu, Al-Mulla, Fahd, Bapat, Bharati, Bernstein, Inge, Capellá, Gabriel, den Dunnen, Johan T, du Sart, Desiree, Fabre, Aurelie, Farrell, Michael P, Farrington, Susan M, Frayling, Ian M, Frebourg, Thierry, Goldgar, David E, Heinen, Christopher D, Holinski-Feder, Elke, Kohonen-Corish, Maija, Robinson, Kristina Lagerstedt, Leung, Suet Yi, Martins, Alexandra, Moller, Pal, Morak, Monika, Nystrom, Minna, Peltomaki, Paivi, Pineda, Marta, Qi, Ming, Ramesar, Rajkumar, Rasmussen, Lene Juel, Royer-Pokora, Brigitte, Scott, Rodney J, Sijmons, Rolf, Tavtigian, Sean V, Tops, Carli M, Weber, Thomas, Wijnen, Juul, Woods, Michael O, Macrae, Finlay, Genuardi, Maurizio, Castillejo, Adela, Sexton, Adrienne, Chan, Anthony K W, Viel, Alessandra, Blanco, Amie, French, Amy, Laner, Andreas, Wagner, Anja, van den Ouweland, Ans, Mensenkamp, Arjen, Payá, Artemio, Betz, Beate, Redeker, Bert, Smith, Betsy, Espenschied, Carin, Cummings, Carole, Engel, Christoph, Fornes, Claudia, Valenzuela, Cristian, Alenda, Cristina, Buchanan, Daniel, Barana, Daniela, Konstantinova, Darina, Cairns, Dianne, Glaser, Elizabeth, Silva, Felipe, Lalloo, Fiona, Crucianelli, Francesca, Hogervorst, Frans, Casey, Graham, Tomlinson, Ian, Blanco, Ignacio, Villar, Isabel López, Garcia-Planells, Javier, Bigler, Jeanette, Shia, Jinru, Martinez-Lopez, Joaquin, Gille, Johan J P, Hopper, John, Potter, John, Soto, José Luis, Kantelinen, Jukka, Ellis, Kate, Mann, Kirsty, Varesco, Liliana, Zhang, Liying, Le Marchand, Loic, Marafie, Makia J, Nordling, Margareta, Tibiletti, Maria Grazia, Kahan, Mariano Ariel, Ligtenberg, Marjolijn, Clendenning, Mark, Jenkins, Mark, Speevak, Marsha, Digweed, Martin, Kloor, Matthias, Hitchins, Megan, Myers, Megan, Aronson, Melyssa, Valentin, Mev Dominguez, Kutsche, Michael, Parsons, Michael, Walsh, Michael, Kansikas, Minttu, Zahary, Mohd Nizam, Pedroni, Monica, Heider, Nao, Poplawski, Nicola, Rahner, Nils, Lindor, Noralane M, Sala, Paola, Nan, Peng, Propping, Peter, Newcomb, Polly, Sarin, Rajiv, Haile, Robert, Hofstra, Robert, Ward, Robyn, Tricarico, Rossella, Bacares, Ruben, Young, Sean, Chialina, Sergio, Kovalenko, Serguei, Gunawardena, Shanaka R, Moreno, Sira, Ho, Siu Lun, Yuen, Siu Tsan, Thibodeau, Stephen N, Gallinger, Steve, Burnett, Terrilea, Teitsch, Therese, Chan, Tsun Leung, Smyrk, Tom, Cranston, Treena, Psofaki, Vasiliki, Steinke-Lange, Verena, Barbera, Victor-Manuel
Publikováno v:
Recercat. Dipósit de la Recerca de Catalunya
instname
Nature Genetics
Nature Genetics, Nature Publishing Group, 2014, 46 (2), pp.107-115. ⟨10.1038/ng.2854⟩
Nature Genetics, 46(2), 107
Nature Genetics, 46, 107-15
Nature genetics, 46(2), 107-115. Nature Publishing Group
Nature Genetics, 46(2), 107-+. Nature Publishing Group
Thompson, B A, Spurdle, A B, Plazzer, J-P, Greenblatt, M S, Akagi, K, Al-Mulla, F, Bapat, B, Bernstein, I, Capellá, G, den Dunnen, J T, du Sart, D, Fabre, A, Farrell, M P, Farrington, S M, Frayling, I M, Frebourg, T, Goldgar, D E, Heinen, C D, Holinski-Feder, E, Kohonen-Corish, M, Robinson, K L, Leung, S Y, Martins, A, Moller, P, Morak, M, Nystrom, M, Peltomaki, P, Pineda, M, Qi, M, Ramesar, R, Rasmussen, L J, Royer-Pokora, B, Scott, R J, Sijmons, R, Tavtigian, S V, Tops, C M, Weber, T, Wijnen, J, Woods, M O, Macrae, F, Genuardi, M, Castillejo, A, Sexton, A, Chan, A K W, Viel, A, Blanco, A, French, A, Laner, A, Wagner, A, van den Ouweland, A & on behalf of InSiGHT 2014, ' Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database ', Nature Genetics, vol. 46, no. 2, pp. 107-115 . https://doi.org/10.1038/ng.2854
Dipòsit Digital de la UB
Universidad de Barcelona
Nature Genetics, 46, 2, pp. 107-15
Nature Genetics, 46(2), 107-115.e2. Nature Publishing Group
instname
Nature Genetics
Nature Genetics, Nature Publishing Group, 2014, 46 (2), pp.107-115. ⟨10.1038/ng.2854⟩
Nature Genetics, 46(2), 107
Nature Genetics, 46, 107-15
Nature genetics, 46(2), 107-115. Nature Publishing Group
Nature Genetics, 46(2), 107-+. Nature Publishing Group
Thompson, B A, Spurdle, A B, Plazzer, J-P, Greenblatt, M S, Akagi, K, Al-Mulla, F, Bapat, B, Bernstein, I, Capellá, G, den Dunnen, J T, du Sart, D, Fabre, A, Farrell, M P, Farrington, S M, Frayling, I M, Frebourg, T, Goldgar, D E, Heinen, C D, Holinski-Feder, E, Kohonen-Corish, M, Robinson, K L, Leung, S Y, Martins, A, Moller, P, Morak, M, Nystrom, M, Peltomaki, P, Pineda, M, Qi, M, Ramesar, R, Rasmussen, L J, Royer-Pokora, B, Scott, R J, Sijmons, R, Tavtigian, S V, Tops, C M, Weber, T, Wijnen, J, Woods, M O, Macrae, F, Genuardi, M, Castillejo, A, Sexton, A, Chan, A K W, Viel, A, Blanco, A, French, A, Laner, A, Wagner, A, van den Ouweland, A & on behalf of InSiGHT 2014, ' Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database ', Nature Genetics, vol. 46, no. 2, pp. 107-115 . https://doi.org/10.1038/ng.2854
Dipòsit Digital de la UB
Universidad de Barcelona
Nature Genetics, 46, 2, pp. 107-15
Nature Genetics, 46(2), 107-115.e2. Nature Publishing Group
Contains fulltext : 138857.pdf (Publisher’s version ) (Closed access) The clinical classification of hereditary sequence variants identified in disease-related genes directly affects clinical management of patients and their relatives. The Internat