A novel STK11 germline mutation in two siblings with Peutz-Jeghers syndrome complicated by primary gastric cancer
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2005.00380.x/fullpdf
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3. Familial gastric cancer: clinicopathological characteristics, RER phenotype and germline p53 and E-cadherin mutations;Shinmura;Carcinogenesis,1999
4. E-cadherin gene variants in gastric cancer families whose probands are diagnosed with diffuse gastric cancer;Yabuta;Int J Cancer,2002
5. Ile-Leu substitution (I415L) in germline E-cadherin gene (CDH1) in Japanese familial gastric cancer;Wang;Jpn J Clin Oncol,2003
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1. Pathological Diagnosis and Classification of Gastric Epithelial Tumours;Current Clinical Pathology;2019
2. Seven-Year Follow-Up of Peutz-Jeghers Syndrome;Case Reports in Dentistry;2016
3. Peutz-Jeghers Syndrome With Diffuse Gastrointestinal Polyposis: Three Cases in a Family With Different Manifestations and No Evidence of Malignancy During 14 Years Follow Up;Iranian Red Crescent Medical Journal;2015-12-19
4. Recognition of and recent issues in hereditary diffuse gastric cancer;Journal of Gastroenterology;2015-06-07
5. STK11Domain XI Mutations: Candidate Genetic Drivers Leading to the Development of Dysplastic Polyps in Peutz-Jeghers Syndrome;Human Mutation;2014-06-03
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