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Increasing Lynch Syndrome Identification Through Establishment of a Hereditary Colorectal Cancer RegistrySTURGEON, Duveen; MCCUTCHEON, Tonna; GEIGER, Timothy M et al.Diseases of the colon & rectum. 2013, Vol 56, Num 3, pp 308-314, issn 0012-3706, 7 p.Article

Report on de-novo mutation in the MSH2 gene as a rare event in hereditary nonpolyposis colorectal cancerMORAK, Monika; LANER, Andreas; SCHOLZ, Michael et al.European journal of gastroenterology & hepatology. 2008, Vol 20, Num 11, pp 1101-1105, issn 0954-691X, 5 p.Article

Adherence to Microsatellite Instability Testing in Young-Onset Colorectal Cancer PatientsKESSELS, Koen; FIDDER, Herma H; DE GROOT, Nicolette L et al.Diseases of the colon & rectum. 2013, Vol 56, Num 7, pp 825-833, issn 0012-3706, 9 p.Article

Laparoscopic Low Anterior Resection in a Patient With Lynch Syndrome and Previous Right HemicolectomyKELLER, D. S; LAWRENCE, J. K; DELANEY, C. P et al.Diseases of the colon & rectum. 2013, Vol 56, Num 2, issn 0012-3706, p. 263Article

Spectrum of MLH1 and MSH2 Mutations in Chilean Families With Suspected Lynch SyndromeALVAREZ, Karin; HURTADO, Claudia; HEVIA, Montserrat A et al.Diseases of the colon & rectum. 2010, Vol 53, Num 4, pp 450-459, issn 0012-3706, 10 p.Article

Somatic Mutations of the CDC4 (FBXW7) Gene in Hereditary Colorectal TumorsMIYAKI, Michiko; YAMAGUCHI, Tatsuro; LIJIMA, Takeru et al.Oncology. 2009, Vol 76, Num 6, pp 430-434, issn 0030-2414, 5 p.Article

Identification and Classification of Hereditary Nonpolyposis Colorectal Cancer (Lynch Syndrome) : Adapting Old Concepts to Recent Advancements. Report from the Italian Association for the Study of Hereditary Colorectal Tumors Consensus GroupPONZ DE LEON, Maurizio; BERTARIO, Lucio; GENUARDI, Maurizio et al.Diseases of the colon & rectum. 2007, Vol 50, Num 12, pp 2126-2134, issn 0012-3706, 9 p.Article

Is the Phenotype Mixed or Mistaken? Hereditary Nonpolyposis Colorectal Cancer and Hyperplastic Polyposis SyndromeJARRAR, Awad M; CHURCH, James M; FAY, Susan et al.Diseases of the colon & rectum. 2009, Vol 52, Num 12, pp 1949-1955, issn 0012-3706, 7 p.Article

Unusual DNA mismatch repair―deficient tumors in Lynch syndrome: a report of new cases and review of the literatureKARAMURZIN, Yevgeniy; ZHAOSHI ZENG; PATY, Philip B et al.Human pathology. 2012, Vol 43, Num 10, pp 1677-1687, issn 0046-8177, 11 p.Article

Lynch syndrome in Tunisia: first description of clinical features and germline mutationsAISSI-BEN MOUSSA, Sana; MOUSSA, Amel; MANAI, Mohamed et al.International journal of colorectal disease (Print). 2011, Vol 26, Num 4, pp 455-467, issn 0179-1958, 13 p.Article

Solitary Subungual Keratoacanthoma Arising in an MSH2 Germline Mutation Carrier: Confirmation of a Relationship by Immunohistochemical AnalysisSTOEBNER, P. E; FABRE, C; DELFOUR, C et al.Dermatology (Basel). 2009, Vol 219, Num 2, pp 174-178, issn 1018-8665, 5 p.Article

Early Carcinogenic Events in HNPCC Adenomas : Differences with Sporadic AdenomasRIJCKEN, Fleur Elise Marie; KOORNSTRA, Jan Jacob; VAN DER SLUIS, Tineke et al.Digestive diseases and sciences. 2008, Vol 53, Num 6, pp 1660-1668, issn 0163-2116, 9 p.Article

Immunohistochemistry to Detect Hereditary Nonpolyposis Colorectal Cancer in Young Patients: the 7-Year Auckland ExperienceWRIGHT, Deborah M; ARNOLD, Julie L; PARRY, Bryan et al.Diseases of the colon & rectum. 2011, Vol 54, Num 5, pp 552-558, issn 0012-3706, 7 p.Article

Colon Cancer Screening Practices and Disclosure After Receipt of Positive or Inconclusive Genetic Test Results for Hereditary Nonpolyposis Colorectal CancerERSIG, Anne L; HADLEY, Donald W; KOEHLY, Laura M et al.Cancer. 2009, Vol 115, Num 18, pp 4071-4079, issn 0008-543X, 9 p.Article

Malignant melanoma in patients with hereditarynonpolyposis colorectal cancerPONTI, G; LOST, L; PELLACANI, G et al.British journal of dermatology (1951). 2008, Vol 159, Num 1, pp 162-168, issn 0007-0963, 7 p.Article

Randomized Trial of a Decision Aid for Individuals Considering Genetic Testing for Hereditary Nonpolyposis Colorectal Cancer RiskWAKEFIELD, Claire E; MEISER, Bettina; HOMEWOOD, Judi et al.Cancer. 2008, Vol 113, Num 5, pp 956-965, issn 0008-543X, 10 p.Article

Consideration of Hereditary Nonpolyposis Colorectal Cancer in BRCA Mutation-Negative Familial Ovarian CancersSOUTH, Stacey A; VANCE, Heidi; FARRELL, Carolyn et al.Cancer. 2009, Vol 115, Num 2, pp 324-333, issn 0008-543X, 10 p.Article

Intraductal Papillary Mucinous Neoplasm of the Pancreas With Loss of Mismatch Repair in a Patient With Lynch SyndromeSPARR, Jennifer A; BANDIPALLIAM, Prathap; REDSTON, Mark S et al.The American journal of surgical pathology. 2009, Vol 33, Num 2, pp 309-312, issn 0147-5185, 4 p.Article

Preferences for Outcomes Associated With Decisions to Undergo or Forgo Genetic Testing for Lynch SyndromeKUPPERMANN, Miriam; WANG, Grace; WONG, Shirley et al.Cancer. 2013, Vol 119, Num 1, pp 215-225, issn 0008-543X, 11 p.Article

Development and validation of an instrument to measure the impact of genetic testing on self-concept in Lynch syndromeESPLEN, M. J; STUCKLESS, N; PETERSEN, H. V et al.Clinical genetics. 2011, Vol 80, Num 5, pp 415-423, issn 0009-9163, 9 p.Article

Analysis of EPCAM Protein Expression in Diagnostics of Lynch SyndromeKLOOR, Matthias; VOIGT, Anita Y; SCHACKERT, Hans K et al.Journal of clinical oncology. 2011, Vol 29, Num 2, pp 223-227, issn 0732-183X, 5 p.Article

A frame-shift mutation of PMS2 is a widespread cause of Lynch syndromeCLENDENNING, M; SENTER, L; LINDBLOM, A et al.Journal of medical genetics. 2008, Vol 45, Num 6, pp 340-345, issn 0022-2593, 6 p.Article

Population-Based Molecular Screening for Lynch Syndrome: Implications for Personalized MedicineWARD, Robyn L; HICKS, Sian; HAWKINS, Nicholas J et al.Journal of clinical oncology. 2013, Vol 31, Num 20, pp 2554-2562, issn 0732-183X, 9 p.Article

Le Syndrome de Lynch: pathologiste et praticien peuvent ensemble réduire le risque de cancer : PATHOLOGIE POUR LE PRATICIEN = Lynch Syndrome: when pathologist and clinician have the opportunity to reduce the risk of developing cancerGENEVAY, M; BENUSIGLIO, P. R; HUTTER, P et al.Revue médicale suisse. 2011, Vol 7, Num 303, pp 1502-1506, issn 1660-9379, 5 p.Article