Clinical utility gene card for: Lynch syndrome (MLH1, MSH2, MSH6, PMS2).
作者信息
Rahner Nils, Steinke Verena, Schlegelberger Brigitte, Olschwang Sylviane, Eisinger François, Hutter Pierre
机构信息
Institute of Human Genetics, University of Bonn, Bonn, Germany.
出版信息
Eur J Hum Genet. 2010 Sep;18(9). doi: 10.1038/ejhg.2009.232. Epub 2010 Jan 27.
Abstract
摘要
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本文引用的文献
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Calculation of risk of colorectal and endometrial cancer among patients with Lynch syndrome.林奇综合征患者结直肠癌和子宫内膜癌风险的计算。
Gastroenterology. 2009 Nov;137(5):1621-7. doi: 10.1053/j.gastro.2009.07.039. Epub 2009 Jul 18.
2
Genetic testing in gastroenterology: Lynch syndrome.胃肠病学中的基因检测：林奇综合征
Best Pract Res Clin Gastroenterol. 2009;23(2):185-96. doi: 10.1016/j.bpg.2009.02.006.
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Incorporation of somatic BRAF mutation testing into an algorithm for the investigation of hereditary non-polyposis colorectal cancer.将体细胞BRAF突变检测纳入遗传性非息肉病性结直肠癌的诊断流程。
Fam Cancer. 2007;6(3):301-10. doi: 10.1007/s10689-007-9124-1. Epub 2007 Apr 24.
4
Prognostic value of Y deletion analysis: what is the clinical prognostic value of Y chromosome microdeletion analysis?Y染色体缺失分析的预后价值：Y染色体微缺失分析的临床预后价值是什么？
Hum Reprod. 2000 Jul;15(7):1431-4. doi: 10.1093/humrep/15.7.1431.
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A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer.美国国立癌症研究所微卫星不稳定性用于癌症检测和家族易感性研讨会：制定结直肠癌微卫星不稳定性测定的国际标准。
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