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临床分子诊断实验室的质量管理(英文)
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作者 Tian-jian CHEN Yue-ying WANG xi-yu he 《北京大学学报(医学版)》 CAS CSCD 北大核心 2006年第1期30-32,共3页
After completion of the human genome project, health professionals and the public become more aware aboutthe role of genetic information in medical practice. We are in a transition period to enter a new“genomic medi-... After completion of the human genome project, health professionals and the public become more aware aboutthe role of genetic information in medical practice. We are in a transition period to enter a new“genomic medi-cine”era[1,2]. In the past two decades, many mutations at disease causing genes have been identified and correla-ted to clinical phenotypes. Molecular diagnostic tests for such mutations have been developed and shown their pro-found impacts on clinical medicine and public health. With the development of new genomic technologies, large-scale analysis of human genome and transcriptome are become possible. For example,microarray analysis allows as-sessment of entire expression profile of cancer. By integrating of information from genome and expression profileswith clinical data, cancer molecular classification will become a powerful clinical tool to correlation cancers withtheir prognostics, sensitivity to chemotherapy, and the potential of metastasis[3]. Thus, molecular diagnosis will be-come important soon for clinical physicians and cancer patients on selection of the optimal healthcare approaches. 展开更多
关键词 分子诊断 实验室 医院 质量控制 全面质量管理
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