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J-GLOBAL ID:201802281432923534   Reference number:18A1420693

リンチ症候群のスクリーニング

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Material:
Volume: 66  Issue:Page: 221-223(J-STAGE)  Publication year: 2018 
JST Material Number: G0594A  ISSN: 0037-3826  CODEN: SIZAA7  Document type: Article
Article type: 解説  Country of issue: Japan (JPN)  Language: JAPANESE (JA)
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JST classification (4):
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Category name(code) classified by JST.
Diagnostics of congenital diseases, deformities.  ,  Tumors(=neoplasms)of digestive system  ,  Diagnosis of tumors(=neoplasms)  ,  Medical examinations in general 
Reference (5):
  • 1) Lynch HT, de la Chapelle A : Hereditary colorectal cancer. N Engl J Med 348 : 919-932, 2003
  • 2) Bonadona V, Bonaiti B, Olschwang S, et al. : Cancer risks associated with germline mutation in MLH1, MSH2 and MSH6 genes in Lynch syndrome. JAMA 305 : 2304-2310, 2011
  • 3) The international Collaborative Group on Hereditary Non Polyposis Colorectal Cancer (ICG-HNPCC) http://www.insight-group.org/
  • 4) 遺伝性大腸癌診療ガイドライン2016年版http://www.jsccr.jp/guideline/2016/hereditary_particular.html#no2-5
  • 5) Shia J, Tang LH, Vakiani E, Guillem JG, Stadler ZK, Soslow RA, Katabi N, Weiser MR, Paty PB, Temple LK, Nash GM, Wong WD, Offit K, Klimstra DS : Immunohistochemistry as first-line screening for detecting colorectal cancer patients at risk for hereditary nonpolyposis colorectal cancer syndrome : a 2-antibody panel may be as predictive as a 4-antibody panel. Am J Surg Pathol 33 : 1639-1645, 2009
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