Duodenal adenocarcinoma and Mut Y human homologue-associated polyposis
暂无分享,去创建一个
[1] P. Propping,et al. MUTYH‐associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype , 2006, International journal of cancer.
[2] P. Chappuis,et al. Prevalence of MYH germline mutations in Swiss APC mutation‐negative polyposis patients , 2006, International journal of cancer.
[3] R. Écochard,et al. Surveillance of duodenal adenomas in familial adenomatous polyposis reveals high cumulative risk of advanced disease. , 2004, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[4] Siân Jones,et al. Autosomal recessive colorectal adenomatous polyposis due to inherited mutations of MYH , 2003, The Lancet.
[5] L. Lipton,et al. Multiple colorectal adenomas, classic adenomatous polyposis, and germ-line mutations in MYH. , 2003, The New England journal of medicine.
[6] Alison L. Livingston,et al. Inherited variants of MYH associated with somatic G:C→T:A mutations in colorectal tumors , 2002, Nature Genetics.
[7] K. Kinzler,et al. The molecular basis of Turcot's syndrome. , 1995, The New England journal of medicine.
[8] R. Phillips,et al. Surveillance and management of upper gastrointestinal disease in Familial Adenomatous Polyposis , 2005, Familial Cancer.