机译:在基于汉族的中国汉族人群中,IL10基因启动子区多态性-592A / C与图雷特氏综合症之间缺乏关联
Shandong Provincial Key Laboratory of Metabolic Disease, The Affiliated Hospital of Medical College, Qingdao University, Qingdao, China,Institute of Clinical Research, The Affiliated Hospital of Medical College, Qingdao University, Qingdao, China,Genetic Laboratory, The Affiliated Hospital of Medical College, Qingdao University, Qingdao, China;
Child Healthcare Department, The Affiliated Hospital of Medical College, Qingdao University, Qingdao, China;
Medical School, Qingdao University, Qingdao, China;
Neurology Department, The Affiliated Linyi People's Hospital, Shandong University, Linyi, China,Neurology Department The Affiliated Linyi People's Hospital Shandong University Shandong Provence 27 Jiefang Road Linyi 276000 China;
Graduate School, Peking Union Medical College, Beijing, China,Center for Genetics, National Research Institute for Family Planning, Beijing, China,World Health Organization Collaborating Centre for Research in Human Reproduction, Beijing, China,Center for Genetics National Research Institute for Family Planning 12, Dahuisi Road Haidian Beijing 100081 China;
机译:IL10基因启动子区多态性-592A / C与中国汉族人群强迫症缺乏关联
机译:IL10基因启动子区多态性-592A / C与中国汉族人群强迫症缺乏关联
机译:在中国汉族人群的基于家庭的关联研究中,缺乏5-HTR2A 102 T / C和-1438A / G多态性与图雷特综合征的遗传关联
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:牛热休克蛋白70基因启动子区域内单核苷酸多态性的鉴定及其与妊娠的关系
机译:中国汉族人群中精神分裂症1(DISC1)基因多态性与自闭症之间关联的证据:基于家庭的关联研究
机译:中国汉族人群中精神分裂症1(DISC1)基因多态性与自闭症之间关联的证据:基于家庭的关联研究