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Nature Reviews Gastroenterology & Hepatology, ISSN 1759-5045, 09/2013, Volume 10, Issue 9, pp. 506 - 508
Jasperson, K. Nat. Rev. Gastroenterol. Hepatol. 10, 506-508 (2013); published online 9 July 2013; doi: 10.1038/nrgastro.2013.122 
Usage | Colorectal cancer | Genetic aspects | Diagnosis | Research | Risk factors | Genetic screening
Journal Article
Nature reviews. Gastroenterology & hepatology, ISSN 1759-5045, 2013, Volume 10, Issue 9, pp. 506 - 508
Genetic testing in relatives of individuals with Lynch syndrome is of utmost importance for targeted screening and prevention. A recent systematic review... 
GASTROENTEROLOGY & HEPATOLOGY | STRATEGIES | Patient Acceptance of Health Care - statistics & numerical data | Colorectal Neoplasms, Hereditary Nonpolyposis - diagnosis | Genetic Testing - utilization | Humans
Journal Article
Human Pathology, ISSN 0046-8177, 2015, Volume 49, pp. 39 - 48
Journal Article
International Journal of Colorectal Disease, ISSN 0179-1958, 3/2016, Volume 31, Issue 3, pp. 711 - 712
To access, purchase, authenticate, or subscribe to the full-text of this article, please visit this link: http://dx.doi.org/10.1007/s00384-015-2204-z 
Internal Medicine | Medicine & Public Health | Surgery | Hepatology | Gastroenterology | Proctology | SURGERY | GASTROENTEROLOGY & HEPATOLOGY | Female | Rectal Neoplasms - genetics | DNA-Binding Proteins - genetics | Nuclear Proteins - genetics | Humans | Adaptor Proteins, Signal Transducing - genetics
Journal Article
JAMA, ISSN 0098-7484, 03/2016, Volume 315, Issue 12, pp. 1266 - 1275
Journal Article
Application of Clinical Genetics, ISSN 1178-704X, 07/2016, Volume 9, pp. 83 - 92
Cowden syndrome (CS) is an often difficult to recognize hereditary cancer predisposition syndrome caused by mutations in phosphatase and tensin homolog deleted... 
Cowden syndrome | PTEN gene | Genetic counseling | Hereditary cancer | Genetic aspects | Skin | Phosphatases | Research | Diagnostic equipment (Medical) | Mutation | Kinases | Health risk assessment | Womens health
Journal Article
Cancer Journal (United States), ISSN 1528-9117, 07/2012, Volume 18, Issue 4, pp. 328 - 333
Journal Article
Surgical Oncology Clinics of North America, ISSN 1055-3207, 10/2015, Volume 24, Issue 4, pp. 683 - 703
Journal Article
Familial Cancer, ISSN 1389-9600, 6/2014, Volume 13, Issue 2, pp. 257 - 265
Journal Article
American Journal of Gastroenterology, ISSN 0002-9270, 10/2017, Volume 112, pp. S46 - S47
Journal Article
Journal of Genetic Counseling, ISSN 1059-7700, 8/2012, Volume 21, Issue 4, pp. 484 - 493
Identifying individuals who have Lynch syndrome (LS) involves a complex diagnostic work up that includes taking a detailed family history and a combination of... 
Human Genetics | Immunohistochemistry | Gynecology | Clinical Psychology | Public Health/Gesundheitswesen | Colorectal neoplasms | Microsatellite instability | Ethics | Practice guideline | Biomedicine | Genetic testing | DNA mismatch repair | Lynch syndrome | Uterine neoplasms | COST-EFFECTIVENESS | ENDOMETRIAL CANCER | STRATEGIES | COLON-CANCER | LATER AGE | HNPCC | PREDISPOSITION | FAMILIES | GENETICS & HEREDITY | Antigens, Neoplasm - genetics | MutL Protein Homolog 1 | Cell Adhesion Molecules - genetics | Genetic Predisposition to Disease | Microsatellite Instability | Genetic Testing | Colorectal Neoplasms - genetics | Colorectal Neoplasms, Hereditary Nonpolyposis - genetics | Colorectal Neoplasms, Hereditary Nonpolyposis - pathology | Humans | DNA Repair Enzymes - genetics | Base Pair Mismatch | DNA-Binding Proteins - genetics | Genetic Counseling | Epithelial Cell Adhesion Molecule | DNA Methylation | Societies, Medical | Proto-Oncogene Proteins B-raf - genetics | DNA Repair | Adaptor Proteins, Signal Transducing - genetics | Adenosine Triphosphatases - genetics | Mismatch Repair Endonuclease PMS2 | Nuclear Proteins - genetics | Oncology, Experimental | Colorectal cancer | Practice guidelines (Medicine) | Research | Genetic screening | Preventive health services | Algorithms | Nurses | Gastrointestinal diseases | DNA | Medical genetics | Medicine, Preventive | Trade and professional associations | Cancer | Tumors | Data processing | Genetic counselling | Joints
Journal Article
Familial Cancer, ISSN 1389-9600, 4/2019, Volume 18, Issue 2, pp. 197 - 201
Whether monoallelic MUTYH mutations increase female breast cancer risk remains controversial. This study aimed to determine if monoallelic MUTYH mutations are... 
Human Genetics | Biomedicine, general | Multigene panel testing | Monoallelic MUTYH | Biomedicine | MUTYH carrier | Colorectal cancer | Cancer Research | Breast cancer | Epidemiology | VARIANTS | GENE | ONCOLOGY | COLORECTAL-CANCER | POLYPOSIS | GENETICS & HEREDITY | MUTATIONS | Yuan (China) | Oncology, Experimental | Research | Health aspects | Risk factors | Cancer | Hormone replacement therapy | Mutation | Health risk assessment
Journal Article
Familial Cancer, ISSN 1389-9600, 1/2019, Volume 18, Issue 1, pp. 105 - 108
Constitutional mismatch repair deficiency (CMMRD) syndrome is a rare autosomal recessive hereditary cancer condition, characterized by an exceptionally high... 
Human Genetics | Biomedicine, general | MSH6 | CMMRD | Biomedicine | Constitutional mismatch repair deficiency syndrome | Hereditary brain tumor | Cancer Research | Hereditary breast cancer | Epidemiology | Lynch syndrome | RISKS |