Dissertation　

About 45 item dissertation in line with SLC26A4 query results,the following is 1 to 50(Search took 0.050 seconds)

  1. Clinical Research on Newborn Hearing Concurrent Genetic Screening in106,513Neonates and New Technology Development,HanBing/,0/87
  2. Analyze the Situation of Newborn Hearing and Deafness Gene Screening in Tianjin,LiuShuang/Tianjin Medical University,0/7
  3. 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
  4. Genetic Testing and Mutation Analysis for the Cochlear Implantation Children and Their Normal Auditory Phenotype Parents,ShiMing/,0/31
  5. Deafness Gene Analysis of129Patients with Non-syndromic Deafness in Taiyuan,ZhangQiangWei/Shanxi Medical,0/37
  6. Clinical Diagnosis of Targe Vestibular Aqueduct Syndrome and Cochlear Intervention,JinPeng/Jilin University,0/29
  7. Chinese Population-Specific Deafness Related Genes SLC26A4Gene Variation of Pathogenic Identification and Their Deaf Mechanism,ZhangGuoZheng/Hebei Medical University,0/39
  8. Study on the Etiological Factors,Molecular Pathogenesis and Racial Diversity of Hearing Loss in Profound Hearing Loss Children,LaiRuoSha/Central South University,0/124
  9. SLC26A4, TFAM Gene Polymorphism and Late-onset Alzheimer’s Disease in a Han Chinese Population,ZhangJiFang/Ocean University of China,0/49
  10. Auditory Screening Concurrent Deafness Predisposing Genes Screening in10,043Neonates in Gansu Province,ZhangZheWen/Lanzhou University,0/73
  11. Clinical Practice of Genetic Testing for Hearing Loss,WangGuoJian/PLA Postgraduate Medical School,4/562
  12. The Study of Deafness Molecular Diagnosis Technology in Clinical Application,HanMingZuo/PLA Postgraduate Medical School,2/154
  13. 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
  14. Study on Molecular Epidemiology and Pathogenesis of Severe to Profound Hearing Loss in China,YuanYongYi/PLA Postgraduate Medical School,7/365
  15. 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
  16. 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
  17. 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
  18. The Auditory Characters for Newborns & Infants and the Deaf Gene Mutations and Genotype-Phenotype Correlations in Shandong Province,LinZuo/Shandong University,1/138
  19. HRCT Analysis of Inner Ear Malformation and Deafness Gene Mutations in Chinese Pedigrees with SNHL,MaXiuFang/Shandong University,0/167
  20. Molecular Genetic Analysis of Chinese Hearing Loss Population,HuHao/Central South University,0/189
  21. Mutation Detection and Functional Study of Related Genes of Enlarged Vestibular Aqueduct Syndrome,MeiLingYun/Central South University,1/118
  22. Molecular Genetic Analysis of Waardenburg Syndrome and Non-syndromic Hearing Loss,ChenHongSheng/Central South University,0/125
  23. Comparison and Analysis of Common Mutations in Uighur and Han Patients with Non-syndromic Deafness in Xinjiang,ChenYu/Xinjiang Medical University,0/80
  24. 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
  25. 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
  26. Study on the Hot Spot Mutation of SLC26A4 Gene and LVAS in Sensorineural Hearing Loss with Unknown Reason,NengLingLing/Zhengzhou University,3/52
  27. Molecular Epidemiology Investigation of Common Deafness Genes in Chinese Northwest,XuBaiCheng/Lanzhou University,0/140
  28. Genetic Counseling and Prenatal Diagnosis for Hearing Loss Based on Genetic Testing,HanBing/PLA Postgraduate Medical School,1/277
  29. Molecular Epidemiology Investigation of Enlarged Vestibular Aqueduct Associated with SLC26A4 Gene,ZhaoYaLi/PLA Postgraduate Medical School,9/75
  30. Large vestibular aqueduct syndrome in four cases of clinical analysis and detection of SLC26A4 gene,LiuZhen/Central South University,0/62
  31. Gansu Province deaf students of clinical epidemiology and molecular epidemiological studies,LiuXiaoZuo/Lanzhou University,0/77
  32. Association Studies on Susceptibility Loci (Gene) of Two Types of Non-syndromic Hearing Impairment,ChengHongBo/Nanjing Medical University,0/57
  33. The Clinical Practice on the Concurrent Newborn Hearing and Gene Screening,LiJianQiang/PLA Postgraduate Medical School,0/101
  34. The Molecular Epidemiology Discussion of Newborn Deafness Pathogenic Screening,ZhangDongHong/China Medical University,1/78
  35. Hereditary non- syndromic deafness gene diagnosis system optimization and application,ZhaoJuan/Central South University,0/85
  36. Molecular Epidemiology Investigation of Common Deafness Genes in Deafness Patients of Different Ethnic Origins in Northwest China,ManRongJun/Lanzhou University,0/91
  37. The Molecular Aetiology Study in Non-syndromic Hearing Impairment,HuiPeiLin/Lanzhou University,0/88
  38. The Enforcement and Discussion of Strategy of Newborn Deafness Pathogenic Screening in Shenyang, Liaoning Province of China,QiuHaiTao/China Medical University,0/50
  39. Analysis of the Relatoin between Gene Mutation and Clinical Phenotype for Autosomal Recessive Families,XuZhiYong/Jinan University,0/70
  40. The Epidemiologic Study on Newborn Hearing Combined with Deafness Gene Genotyping in Gansu Province,DingWenJuan/Lanzhou University,0/39
  41. 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
  42. Large vestibular aqueduct syndrome SLC26A4 gene mutations in clinical research,XiHong/Shanxi Medical,0/9
  43. Investigation of SLC26A4 Mutations Associated with Large Vestibular Aqueduct Syndrome and Mondini Dysplasia,ZuoZuo/Hebei Medical University,0/58
  44. Investigation of SLC26A4 Gene in Patients Associated with Sensorineural Hearing Loss in Northwest China,WangYanLi/Lanzhou University,0/39
  45. 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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