Colorectal cancer in Lynch syndrome associated with PMS2 and MSH6 mutations
Author:
Publisher
Springer Science and Business Media LLC
Subject
Gastroenterology
Link
http://link.springer.com/content/pdf/10.1007/s00384-019-03454-4.pdf
Reference10 articles.
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3. Douglas JA, Gruber SB, Meister KA, Bonner J, Watson P, Krush AJ et al (2005) History and molecular genetics of Lynch syndrome in family G: a century later. JAMA 294(17):2195–2202
4. Rohlin A, Rambech E, Kvist A, Torngren T, Eiengard F, Lundstam U, et al (2016). Expanding the genotypephenotype spectrum in hereditary colorectal cancer by gene panel testing. Familial Cancer 16(2):195–203. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5357488/
5. Lucci-Cordisco E, Rovella V, Carrara S, Percesepe A, Pedroni M, Bellacosa A et al (2001) Mutations of the 'minor' mismatch repair gene MSH6 in typical and atypical hereditary nonpolyposis colorectal cancer. Familial Cancer 1(2):93–99
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