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Hereditary Cancer in Clinical Practice, ISSN 1731-2302, 02/2019, Volume 17, Issue 1, pp. 8 - 8
Journal Article
by Dominguez-Valentin, Mev and Sampson, Julian R and Seppälä, Toni T and Ten Broeke, Sanne W and Plazzer, John-Paul and Nakken, Sigve and Engel, Christoph and Aretz, Stefan and Jenkins, Mark A and Sunde, Lone and Bernstein, Inge and Capella, Gabriel and Balaguer, Francesc and Thomas, Huw and Evans, D Gareth and Burn, John and Greenblatt, Marc and Hovig, Eivind and de Vos Tot Nederveen Cappel, Wouter H and Sijmons, Rolf H and Bertario, Lucio and Tibiletti, Maria Grazia and Cavestro, Giulia Martina and Lindblom, Annika and Della Valle, Adriana and Lopez-Köstner, Francisco and Gluck, Nathan and Katz, Lior H and Heinimann, Karl and Vaccaro, Carlos A and Büttner, Reinhard and Görgens, Heike and Holinski-Feder, Elke and Morak, Monika and Holzapfel, Stefanie and Hüneburg, Robert and Knebel Doeberitz, Magnus von and Loeffler, Markus and Rahner, Nils and Schackert, Hans K and Steinke-Lange, Verena and Schmiegel, Wolff and Vangala, Deepak and Pylvänäinen, Kirsi and Renkonen-Sinisalo, Laura and Hopper, John L and Win, Aung Ko and Haile, Robert W and Lindor, Noralane M and Gallinger, Steven and Le Marchand, Loïc and Newcomb, Polly A and Figueiredo, Jane C and Thibodeau, Stephen N and Wadt, Karin and Therkildsen, Christina and Okkels, Henrik and Ketabi, Zohreh and Moreira, Leticia and Sánchez, Ariadna and Serra-Burriel, Miquel and Pineda, Marta and Navarro, Matilde and Blanco, Ignacio and Green, Kate and Lalloo, Fiona and Crosbie, Emma J and Hill, James and Denton, Oliver G and Frayling, Ian M and Rødland, Einar Andreas and Vasen, Hans and Mints, Miriam and Neffa, Florencia and Esperon, Patricia and Alvarez, Karin and Kariv, Revital and Rosner, Guy and Pinero, Tamara Alejandra and Gonzalez, María Laura and Kalfayan, Pablo and Tjandra, Douglas and Winship, Ingrid M and Macrae, Finlay and Möslein, Gabriela and Mecklin, Jukka-Pekka and Nielsen, Maartje and Møller, Pål
Genetics in medicine : official journal of the American College of Medical Genetics, ISSN 1098-3600, 07/2019
Pathogenic variants affecting MLH1, MSH2, MSH6, and PMS2 cause Lynch syndrome and result in different but imprecisely known cancer risks. This study aimed to... 
Journal Article
Gastroenterology, ISSN 0016-5085, 11/2018, Volume 155, Issue 5, pp. 1400 - 1409.e2
Journal Article
The Journal of Pathology, ISSN 0022-3417, 10/2017, Volume 243, Issue 2, pp. 242 - 254
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 08/2016, Volume 99, Issue 2, pp. 337 - 351
Journal Article