About 45 item dissertation in line with SLC26A4 query results,the following is 1 to 50(Search took 0.069 seconds)
- Clinical Research on Newborn Hearing Concurrent Genetic Screening in106,513Neonates and New Technology Development,HanBing/The people's Liberation Army Medical Institute Chinese,0/87
- Analyze the Situation of Newborn Hearing and Deafness Gene Screening in Tianjin,LiuShuang/Tianjin Medical University,0/7
- Common Deafness Gene Characteristics Research of Patients with Nonsyndromic Hearing Loss in Tibetan, Tu Nationality and Mongolian in the Northwest of China,YangXiaoLong/Lanzhou University,0/18
- Genetic Testing and Mutation Analysis for the Cochlear Implantation Children and Their Normal Auditory Phenotype Parents,ShiMing/Kunming Medical University,0/31
- Deafness Gene Analysis of129Patients with Non-syndromic Deafness in Taiyuan,ZhangQiangWei/Shanxi Medical,0/37
- Clinical Diagnosis of Targe Vestibular Aqueduct Syndrome and Cochlear Intervention,JinPeng/Jilin University,0/29
- Chinese Population-Specific Deafness Related Genes SLC26A4Gene Variation of Pathogenic Identification and Their Deaf Mechanism,ZhangGuoZheng/Hebei Medical University,0/39
- Study on the Etiological Factors,Molecular Pathogenesis and Racial Diversity of Hearing Loss in Profound Hearing Loss Children,LaiRuoSha/Central South University,0/124
- SLC26A4, TFAM Gene Polymorphism and Late-onset Alzheimer’s Disease in a Han Chinese Population,ZhangJiFang/Ocean University of China,0/49
- Auditory Screening Concurrent Deafness Predisposing Genes Screening in10,043Neonates in Gansu Province,ZhangZheWen/Lanzhou University,0/73
- Clinical Practice of Genetic Testing for Hearing Loss,WangGuoJian/PLA Postgraduate Medical School,4/562
- The Study of Deafness Molecular Diagnosis Technology in Clinical Application,HanMingZuo/PLA Postgraduate Medical School,2/154
- Establishment and Application of Denaturing High Performance Liquid Chromatography Technique Screening SLC26A4 Gene in Chinese Severe-Profound Hearing Impairment Population,ZhuQingWen/PLA Postgraduate Medical School,1/162
- Study on Molecular Epidemiology and Pathogenesis of Severe to Profound Hearing Loss in China,YuanYongYi/PLA Postgraduate Medical School,7/365
- The Analysis of Phonetic Features in Prelingual Deafness Children with Cochlear Implant and the Research about It with Genetic Correlation,LiuYongZhi/Peking Union Medical College , China,0/68
- The Study of Copy Number Variation, KCNJ10 Gene Screening and Expression in Patients with Non-syndromic Enlarged Vestibular Aqueduct,ZhaoJianDong/PLA Postgraduate Medical School,0/97
- The Studies of Epidemiological Characteristics and Impact Factors of the Commone Genes in Patients with Sensorineural Hearing Loss in China,JiYuBin/PLA Postgraduate Medical School,1/196
- The Auditory Characters for Newborns & Infants and the Deaf Gene Mutations and Genotype-Phenotype Correlations in Shandong Province,LinZuo/Shandong University,1/138
- HRCT Analysis of Inner Ear Malformation and Deafness Gene Mutations in Chinese Pedigrees with SNHL,MaXiuFang/Shandong University,0/167
- Molecular Genetic Analysis of Chinese Hearing Loss Population,HuHao/Central South University,0/189
- Mutation Detection and Functional Study of Related Genes of Enlarged Vestibular Aqueduct Syndrome,MeiLingYun/Central South University,1/118
- Molecular Genetic Analysis of Waardenburg Syndrome and Non-syndromic Hearing Loss,ChenHongSheng/Central South University,0/125
- Comparison and Analysis of Common Mutations in Uighur and Han Patients with Non-syndromic Deafness in Xinjiang,ChenYu/Xinjiang Medical University,0/80
- Study and Application of New Diagnostic Techniques on Genetic Deafness Genes and Molecular Genetic Study on a Family with Nonsyndromic Deafness,MenMeiChao/Central South University,0/87
- Study on Inner Ear Malformation for Its Classification and Relationship with SLC26A4 and GJB2 in Patient with Sensorineural Hearing Loss,SunBaoChun/PLA Postgraduate Medical School,0/41
- Study on the Hot Spot Mutation of SLC26A4 Gene and LVAS in Sensorineural Hearing Loss with Unknown Reason,NengLingLing/Zhengzhou University,3/52
- Molecular Epidemiology Investigation of Common Deafness Genes in Chinese Northwest,XuBaiCheng/Lanzhou University,0/140
- Genetic Counseling and Prenatal Diagnosis for Hearing Loss Based on Genetic Testing,HanBing/PLA Postgraduate Medical School,1/277
- Molecular Epidemiology Investigation of Enlarged Vestibular Aqueduct Associated with SLC26A4 Gene,ZhaoYaLi/PLA Postgraduate Medical School,9/75
- Large vestibular aqueduct syndrome in four cases of clinical analysis and detection of SLC26A4 gene,LiuZhen/Central South University,0/62
- Gansu Province deaf students of clinical epidemiology and molecular epidemiological studies,LiuXiaoZuo/Lanzhou University,0/77
- Association Studies on Susceptibility Loci (Gene) of Two Types of Non-syndromic Hearing Impairment,ChengHongBo/Nanjing Medical University,0/57
- The Clinical Practice on the Concurrent Newborn Hearing and Gene Screening,LiJianQiang/PLA Postgraduate Medical School,0/101
- The Molecular Epidemiology Discussion of Newborn Deafness Pathogenic Screening,ZhangDongHong/China Medical University,1/78
- Hereditary non- syndromic deafness gene diagnosis system optimization and application,ZhaoJuan/Central South University,0/85
- Molecular Epidemiology Investigation of Common Deafness Genes in Deafness Patients of Different Ethnic Origins in Northwest China,ManRongJun/Lanzhou University,0/91
- The Molecular Aetiology Study in Non-syndromic Hearing Impairment,HuiPeiLin/Lanzhou University,0/88
- The Enforcement and Discussion of Strategy of Newborn Deafness Pathogenic Screening in Shenyang, Liaoning Province of China,QiuHaiTao/China Medical University,0/50
- Analysis of the Relatoin between Gene Mutation and Clinical Phenotype for Autosomal Recessive Families,XuZhiYong/Jinan University,0/70
- The Epidemiologic Study on Newborn Hearing Combined with Deafness Gene Genotyping in Gansu Province,DingWenJuan/Lanzhou University,0/39
- Molecular Epidemiology Analysis of Deaf-mute Patients in the Co-relationship between SLC26A4 Gene and Enlargement of Vestibular Aqueduct Among Deaf-mute Patierntes in Yunnan Province,FanJianHui/Kunming Medical College,0/14
- Large vestibular aqueduct syndrome SLC26A4 gene mutations in clinical research,XiHong/Shanxi Medical,0/9
- Investigation of SLC26A4 Mutations Associated with Large Vestibular Aqueduct Syndrome and Mondini Dysplasia,ZuoZuo/Hebei Medical University,0/58
- Investigation of SLC26A4 Gene in Patients Associated with Sensorineural Hearing Loss in Northwest China,WangYanLi/Lanzhou University,0/39
- Comparative Studies of DNA Microarray and Sequencing in Genetic Diagnosis on the Patients with Enlarged Vestibular Aqueduct Syndrome,ZhuFaMei/Central South University,0/17
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