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American Journal of Obstetrics and Gynecology, ISSN 0002-9378, 2017, Volume 217, Issue 5, pp. 512 - 521
The world of hereditary cancers has seen exponential growth in recent years. While hereditary breast and ovarian cancer and Lynch syndrome account for the... 
Obstetrics and Gynecology | BRCA | risk reduction | screening | ovarian cancer | high risk | endometrial cancer | hereditary cancer | cervical cancer | Lynch syndrome | Life Sciences & Biomedicine | Obstetrics & Gynecology | Science & Technology | Genetic Testing | DNA Polymerase III - genetics | Hereditary Breast and Ovarian Cancer Syndrome - diagnosis | Humans | Li-Fraumeni Syndrome - diagnosis | DNA Mismatch Repair - genetics | Tumor Suppressor Protein p53 - genetics | Genital Neoplasms, Female - diagnosis | Li-Fraumeni Syndrome - genetics | Epithelial Cell Adhesion Molecule - genetics | Genes, BRCA2 | Female | RNA Helicases - genetics | Lynch Syndrome II - genetics | Neoplastic Syndromes, Hereditary - genetics | Genes, BRCA1 | Genital Neoplasms, Female - genetics | Hereditary Breast and Ovarian Cancer Syndrome - genetics | PTEN Phosphohydrolase - genetics | Genetic Predisposition to Disease | Hamartoma Syndrome, Multiple - genetics | Fanconi Anemia Complementation Group Proteins - genetics | Protein-Serine-Threonine Kinases - genetics | Neoplastic Syndromes, Hereditary - diagnosis | MutS Homolog 2 Protein - genetics | DNA-Binding Proteins - genetics | Peutz-Jeghers Syndrome - genetics | Hamartoma Syndrome, Multiple - diagnosis | MutL Protein Homolog 1 - genetics | Peutz-Jeghers Syndrome - diagnosis | Lynch Syndrome II - diagnosis | Mismatch Repair Endonuclease PMS2 - genetics | Gene mutations | Endometrial cancer | Diagnosis | Cervical cancer | Genetic screening | Cancer | Ovarian cancer | Index Medicus | Abridged Index Medicus
Journal Article
Familial cancer, ISSN 1389-9600, 11/2017, pp. 1 - 6
textabstractPatients synchronously or metachronously presenting with ovarian and colon cancer can pose diagnostic challenges. A primary colon carcinoma can... 
Colon cancer | Lynch syndrome | Ovarian cancer
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, ISSN 1530-0366, 07/2019, Volume 22, Issue 1, pp. 15 - 25
Purpose Pathogenic variants affecting MLH1, MSH2, MSH6, and PMS2 cause Lynch syndrome and result in different but imprecisely known cancer risks. This study... 
MSH6 | PMS2 | MSH2 | MLH1 | MUTATION CARRIERS | Lynch syndrome | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Gender | Health risk assessment | Medical prognosis | Ovarian cancer | Index Medicus
Journal Article
Gastroenterology, ISSN 0016-5085, 2011, Volume 140, Issue 1, pp. 73 - 81.e5
Background & Aims We developed and validated a model to estimate the risks of mutations in the mismatch repair (MMR) genes MLH1 , MSH2 , and MSH6 based on... 
Gastroenterology and Hepatology | Colon Cancer Family Registry | Lynch Syndrome | Prediction Model | Gene-Specific Risk Estimates | Gastroenterology & Hepatology | Life Sciences & Biomedicine | Science & Technology | gene-specific risk estimates | prediction model
Journal Article
Journal Article