학술논문

>>
학술논문
>

'학술논문' 에서의 검색결과 3건 | 목록 1~10

  • 1 .
    Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium
    저자
    by Møller, Pål; Seppälä, Toni; Dowty, James G.; Haupt, Saskia; Dominguez-Valentin, Mev, et al. 
    소스
    Hereditary Cancer in Clinical Practice, 20
    Hereditary cancer in clinical practice, 20:36. BioMed Central Ltd.
    Hereditary Cancer in Clinical Practice, 20(1):36. BioMed Central
    Møller, P, Seppälä, T, Dowty, J G, Haupt, S, Dominguez-Valentin, M, Sunde, L, Bernstein, I, Engel, C, Aretz, S, Nielsen, M, Capella, G, Evans, D G, Burn, J, Holinski-Feder, E, Bertario, L, Bonanni, B, Lindblom, A, Levi, Z, Macrae, F, Winship, I, Plazzer, J P, Sijmons, R, Laghi, L, Valle, A D & The European Hereditary Tumour Group (EHTG) and the International Mismatch Repair Consortium (IMRC) 2022, ' Colorectal cancer incidences in Lynch syndrome : a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium ', Hereditary Cancer in Clinical Practice, vol. 20, no. 1, 36 . https://doi.org/10.1186/s13053-022-00241-1
    European Hereditary Tumour Group (EHTG) and the International Mismatch Repair Consortium (IMRC) 2022, ' Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium ', Hereditary Cancer in Clinical Practice, vol. 20, 36 . https://doi.org/10.1186/s13053-022-00241-1
    Hereditary Cancer in Clinical Practice
    Dipòsit Digital de la UB
    Universidad de Barcelona
    The European Hereditary Tumour Group (EHTG) and the International Mismatch Repair Consortium (IMRC) 2022, ' Colorectal cancer incidences in Lynch syndrome : a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium ', Hereditary Cancer in Clinical Practice, vol. 20, no. 1, 36 . https://doi.org/10.1186/s13053-022-00241-1
    Møller, P, Seppälä, T, Dowty, J G, Haupt, S, Dominguez-Valentin, M, Sunde, L, Bernstein, I, Engel, C, Aretz, S, Nielsen, M, Capella, G, Evans, D G, Burn, J, Holinski-Feder, E, Bertario, L, Bonanni, B, Lindblom, A, Levi, Z, Macrae, F, Winship, I, Plazzer, J-P, Sijmons, R, Laghi, L, Valle, A D, Heinimann, K, Half, E, Lopez-Koestner, F, Alvarez-Valenzuela, K, Scott, R J, Katz, L, Laish, I, Vainer, E, Vaccaro, C A, Carraro, D M, Gluck, N, Abu-Freha, N, Stakelum, A, Kennelly, R, Winter, D, Rossi, B M, Greenblatt, M, Bohorquez, M, Sheth, H, Tibiletti, M G, Lino-Silva, L S, Horisberger, K, Portenkirchner, C, Nascimento, I, Rossi, N T, da Silva, L A, Thomas, H, Zaránd, A, Mecklin, J-P, Pylvänäinen, K, Renkonen-Sinisalo, L, Lepisto, A, Peltomäki, P, Therkildsen, C, Lindberg, L J, Thorlacius-Ussing, O, von Knebel Doeberitz, M, Loeffler, M, Rahner, N, Steinke-Lange, V, Schmiegel, W, Vangala, D, Perne, C, Hüneburg, R, de Vargas, A F, Latchford, A, Gerdes, A-M, Backman, A-S, Guillén-Ponce, C, Snyder, C, Lautrup, C K, Amor, D, Palmero, E, Stoffel, E, Duijkers, F, Hall, M J, Hampel, H, Williams, H, Okkels, H, Lubiński, J, Reece, J, Ngeow, J, Guillem, J G, Arnold, J, Wadt, K, Monahan, K, Senter, L, Rasmussen, L J, van Hest, L P, Ricciardiello, L, Kohonen-Corish, M R J, Ligtenberg, M J L, Southey, M, Aronson, M, Zahary, M N, Samadder, N J, Poplawski, N, Hoogerbrugge, N, Morrison, P J, James, P, Lee, G, Chen-Shtoyerman, R, Ankathil, R, Pai, R, Ward, R, Parry, S, Dębniak, T, John, T, van Overeem Hansen, T, Caldés, T, Yamaguchi, T, Barca-Tierno, V, Garre, P, Cavestro, G M, Weitz, J, Redler, S, Büttner, R, Heuveline, V, Hopper, J L, Win, A K, Lindor, N, Gallinger, S, Le Marchand, L, Newcomb, P A, Figueiredo, J, Buchanan, D D, Thibodeau, S N, Ten Broeke, S W, Hovig, E, Nakken, S, Pineda, M, Dueñas, N, Brunet, J, Green, K, Lalloo, F, Newton, K, Crosbie, E J, Mints, M, Tjandra, D, Neffa, F, Esperon, P, Kariv, R, Rosner, G, Pavicic, W H, Kalfayan, P, Torrezan, G T, Bassaneze, T, Martin, C, Moslein, G, Ahadova, A, Kloor, M, Sampson, J R, Jenkins, M A & European Hereditary Tumour Group (EHTG) and the International Mismatch Repair Consortium (IMRC) 2022, ' Colorectal cancer incidences in Lynch syndrome : a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium ', Hereditary Cancer in Clinical Practice, vol. 20, no. 1, 36 . https://doi.org/10.1186/s13053-022-00241-1
    European Hereditary Tumour Group (EHTG) and the International Mismatch Repair Consortium (IMRC) 2022, ' Colorectal cancer incidences in Lynch syndrome: a comparison of results from the Prospective Lynch Syndrome Database and the International Mismatch Repair Consortium ', Hereditary cancer in clinical practice, vol. 20, no. 1, 36, pp. 36 . https://doi.org/10.1186/s13053-022-00241-1
    The European Hereditary Tumour Group (EHTG) and the International Mismatch Repair Consortium (IMRC) 2022, ' Colorectal cancer incidences in Lynch syndrome : a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium ', Hereditary Cancer in Clinical Practice, vol. 20, 36 . https://doi.org/10.1186/s13053-022-00241-1
    Hereditary Cancer in Clinical Practice, 20, 1
  • 7 .
    Cancer Risks for PMS2-Associated Lynch Syndrome
    저자
    by van Hest, LP; Ten Broeke, Sanne W; Clinical genetics; CCA - Cancer biology and immunology
    소스
    van Hest, LP & Ten Broeke, S W 2018, ' Cancer Risks for PMS2-Associated Lynch Syndrome ', Journal of clinical oncology : official journal of the American Society of Clinical Oncology, vol. 36, no. 29, DOI: 10.1200/JCO.2018.78.4777, pp. 2961-2968 .
    Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 36(29):DOI: 10.1200/JCO.2018.78.4777, 2961-2968. American Society of Clinical Oncology
전체 메뉴 보기