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Germline CHEK2*1100delC mutations in breast cancer patients with multiple primary cancers.

作者信息

Huang J, Domchek S M, Brose M S, Rebbeck T R, Nathanson K L, Weber B L

机构信息

Department of Biology, University of Pennsylvania, Philadelphia, PA, USA.

出版信息

J Med Genet. 2004 Nov;41(11):e120. doi: 10.1136/jmg.2004.022913.

DOI:10.1136/jmg.2004.022913
PMID:15520402
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1735609/
Abstract
摘要

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引用本文的文献

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CHEK2 (∗) 1100delC Mutation and Risk of Prostate Cancer.CHEK2（∗）1100delC突变与前列腺癌风险
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Clinical implications of low-penetrance breast cancer susceptibility alleles.低外显率乳腺癌易感等位基因的临床意义。
Curr Oncol Rep. 2009 Jan;11(1):8-14. doi: 10.1007/s11912-009-0003-9.
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Genetic and functional analysis of CHEK2 (CHK2) variants in multiethnic cohorts.多民族队列中CHEK2（CHK2）变异体的遗传与功能分析。
Int J Cancer. 2007 Dec 15;121(12):2661-7. doi: 10.1002/ijc.23026.
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A multicenter study of cancer incidence in CHEK2 1100delC mutation carriers.CHEK2基因1100delC突变携带者癌症发病率的多中心研究。
Cancer Epidemiol Biomarkers Prev. 2006 Dec;15(12):2542-5. doi: 10.1158/1055-9965.EPI-06-0687.
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CHEK2 1100delC in patients with metachronous cancers of the breast and the colorectum.患有异时性乳腺癌和结直肠癌患者中的CHEK2 1100delC
BMC Cancer. 2006 Mar 15;6:64. doi: 10.1186/1471-2407-6-64.