Molecular screening for Lynch syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
Gastroenterology,Hepatology,General Medicine
Link
http://www.nature.com/articles/ncpgasthep0263.pdf
Reference5 articles.
1. Lynch HT and de la Chapelle A (2003) Hereditary colorectal cancer. N Engl J Med 348: 919–932
2. Truninger K et al. (2005) Immunohistochemical analysis reveals high frequency of PMS2 defects in colorectal cancer. Gastroenterology 128: 1160–1171
3. Umar A et al. (2004) Revised Bethesda guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability. J Natl Cancer Inst 96: 261–268
4. Lindor NM et al. (2005) Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: familial colorectal cancer type X. JAMA 293: 1979–1985
5. Casey G et al. (2005) Conversion analysis for mutation detection in MLH1 and MSH2 in patients with colorectal cancer. JAMA 293: 799–809
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1. Universal screening for Lynch syndrome in operated colorectal cancer by immunohistochemistry: a cohort of patients in Liaoning province, China;European Journal of Cancer Prevention;2023-03-17
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