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机译:肾病酶基因是原发性高血压的新型易感基因:在北方汉族人群中的两阶段关联研究
Department of Evidence Based Medicine and Division of Population Genetics Cardiovascular Institute and Fuwai Hospital Chinese Academy of Medical Sciences and Peking Union Medical College No. 167 Beilishi Road Beijing 100037 China;
Department of Cardiology Peking Union Medical College Hospital Beijing 100730 China;
Tulane University Medical Center New Orleans LA 70112-2699 USA;
Department of Evidence Based Medicine and Division of Population Genetics Cardiovascular Institute and Fuwai Hospital Chinese Academy of Medical Sciences and Peking Union Medical College No. 167 Beilishi Road Beijing 100037 China;
Department of Evidence Based Medicine and Division of Population Genetics Cardiovascular Institute and Fuwai Hospital Chinese Academy of Medical Sciences and Peking Union Medical College No. 167 Beilishi Road Beijing 100037 China;
Department of Evidence Based Medicine and Division of Population Genetics Cardiovascular Institute and Fuwai Hospital Chinese Academy of Medical Sciences and Peking Union Medical College No. 167 Beilishi Road Beijing 100037 China;
Department of Evidence Based Medicine and Division of Population Genetics Cardiovascular Institute and Fuwai Hospital Chinese Academy of Medical Sciences and Peking Union Medical College No. 167 Beilishi Road Beijing 100037 China;
Department of Epidemiology College of Public Health Zhengzhou University Zhengzhou Henan 450052 China;
Department of Evidence Based Medicine and Division of Population Genetics Cardiovascular Institute and Fuwai Hospital Chinese Academy of Medical Sciences and Peking Union Medical College No. 167 Beilishi Road Beijing 100037 China;
National Human Genome Center at Beijing North Yongchang Rd 3-707 Beijing 100176 China;
Department of Evidence Based Medicine and Division of Population Genetics Cardiovascular Institute and Fuwai Hospital Chinese Academy of Medical Sciences and Peking Union Medical College No. 167 Beilishi Road Beijing 100037 China;
Case-control studies; Hypertension; Kidney; Monoamine oxidase; Single nucleotide polymorphism;
机译:瘦素受体基因多态性在原发性高血压易感性中的作用:病例对照协会在北方汉族人群中的研究
机译:北方汉族人群中Mitofusion-2基因多态性与原发性高血压易感性的关系
机译:中国汉族人群eNOS基因rs1800780(A→G)多态性与原发性高血压的遗传相关性
机译:IL-17RC,CHL1,DSCAM和CNTNAP2基因多态性研究中国汉族人群青少年特发性脊柱缺损性研究
机译:使用基于人群的关联研究(病例对照研究)定位近视易感基因。
机译:Emilin1基因与原发性高血压:北方汉族人群的两阶段关联研究
机译:Emilin1基因与原发性高血压:北方汉族人群的两阶段关联研究