About 120 item dissertation in line with Genetic diagnosis query results,the following is 1 to 50(Search took 0.093 seconds)

  1. Epidemiological Investigation of GJB2Gene Hot-spot Mutation in Deafness Disabled Populations in Beijing and Yangzhou of China,PengXin/Yangzhou University,0/27
  2. Using Next-Generation Sequencing as a Genetic Diagnostic Tool in Some Rare Neurological Mendelian Disorders,ChenZhao/Central South University,0/31
  3. The Genotypes of Non-syndromic Oculocutaneous Albinism,PengJie/Central South University,0/39
  4. Screening of Hot-spot Deafness Gene Mutations among Adolescents with Hearing Loss in Yong Chuan,LiuQiZhen/Chongqing Medical University,0/26
  5. Analysis of Clinical Application of Preimplantation Genetic Diagnosis,ZuoXiuHe/Northwest University of Science and Technology,0/122
  6. Deafness Gene Analysis of129Patients with Non-syndromic Deafness in Taiyuan,ZhangQiangWei/Shanxi Medical,0/37
  7. Epidemiological Investigation of SLC26A4Gene Hot-spot Mutation for Enlarged Vestibular Aqueduct in Deafness Disabled Populations in Beijing of China,ZuoLuJie/Hebei Medical University,0/74
  8. Genetic Diagnosis of20Cases with Congenital Indirect Hyperbilirubinemia,ZhangHanBing/Beijing Union Medical College,0/52
  9. Primary Research of Preimplantation Genetic Diagnostic Technique for Marfan Syndrome,NiuZiRu/,0/33
  10. Application of Two Rounds of FISH in Preimplantation Genetic Diagnosis,HaoYan/Anhui Medical University,,0/73
  11. The Investigation of Sperm Fluorescence in Situ Hybridization and Preimplantation Screening on Aneuploidy,ShiQiuZuo/Guangxi Medical University,0/77
  12. Exploration the Method of Y Chromosome Microdeletion Detection by Multiple Displacement Amplification (MDA) and Multiple PCR,ZhuoShengZuo/Tianjin Medical University,0/5
  13. Diagnosis of Patients with Tuberous Sclerosis Complex by Direct Sequencing and MLPA,YanZuo/Central South University,0/86
  14. Detection of β-thalassemia Mutations by Proofreading Polymerase-mediated Mutation-sensitive on/off Switch,LanFen/Nanhua University,0/60
  15. Causes and Therapeutic Strategy of Fertilization Failure in Globozoospermic Patients and Establishment of Genetic Diagnosis Platform for the Disease,ZhuFuXi/Central South University,0/7
  16. The Sutdy on the Gene Tests Service Actuality and Countermeasure of Third-level Hospitals in Hangzhou,ShiLei/Hangzhou Normal University,0/79
  17. A Pilot Study of a Standardized Procedure for Clinical Genetic Counseling in Our Hospital Using Four Cases of Genetic Counseling and Genetic Diagnosis as Examples,HuangLingLi/Central South University,0/234
  18. Study and Application of New Diagnostic Techniques on Deafness Genes and Molecular Epidemiology of Hot-spot Mutations among Non-syndromic Hearing Loss Patients in China,LiZuo/PLA Postgraduate Medical School,1/203
  19. Microfluidic Chip-based Studies on Genentic Diagnosis and Cell-drug Interaction,LiuDaYu/Dalian Institute of Chemical Physics,0/485
  20. Amplification, Cloning and Expression of HIV-1 GAG Gene Fragment and the Purification and Identification of the Expressed Product,JiChangHua/Fourth Military Medical University,0/116
  21. Investigation of Non-Invasive Prenatal Genetic Diagnosis for B Thalassaemia Using Single Fetal Nucleated Erythrocytes from Maternal Blood,WeiHongYing/Guangxi Medical University,0/196
  22. Mutation Study of Oncogene in Multiple Endocrine Neoplasia and Hyperparathyroidism Kindreds,NingZhiWei/Peking Union Medical College , China,0/99
  23. Study on the Genic Identification of Pathogenic Bacteria Responsible for Bacteremia and Enteric Infection,HouXiaoLi/Zhejiang University,0/156
  24. 1. Two Novel Techniques of Screening of Gene Mutations and the Gene Diagnosis of Chinese Hemjophilia B Patients 2. Expression of PAL cDNA from Parsley in Lactococcus Lactis and It’s Application to PKU Gene Therapy as a New Strategy,XiangHua/Peking Union Medical College , China,0/230
  25. The Study of Gene Diagnosis of Monogenic Diseases and It’s Application,ZhongChangGao/Central South University,0/547
  26. Study on the Etiologic Genetic Diagnosis of Antimicrobial-resistant Gram-negative Bacterial Infections,LinDong/Fudan University,0/210
  27. Genetic Heterogeneity and Gene Diagnosis of Autosomal Dominant Polycystic Kidney Disease Using Microsatellite DNA and Single Nucleotide Polymorphisms,ZhangWeiLi/Second Military Medical University,0/200
  28. Study on the Etiological Genetic Diagnosis of Infections Caused by Resistant Gram Positive Cocci,XuXiaoGang/Fudan University,1/271
  29. Elegant Health,ZouShouChang/Hunan Normal University,4/739
  30. The Study on the Gene Diagnose、Molecular Genotype and Resistance Mechanisms of Systemic Candida,LiJinSong/Tianjin Medical University,0/354
  31. Genetic Diagnosis of Down Syndrome and Preliminary Study on Non-Invasive Prenatal Diagnosis of Down Syndrome,ChenZhenBin/Fujian Medical,2/333
  32. Genetic research of 4q35 in facioscapulohumeral muscular dystrophy(FSHD),ZhangJingLi/Postgraduate Medical School,0/37
  33. Genetic Analysis of Nonsyndromic Oculocutaneous Albinism in Chinese Families and Prenatal Genetic Diagnosis of Abinism,LongYan/Peking Union Medical College , China,0/175
  34. Value of Exercise Test in the Diagnosis of Patients with Periodic Paralysis,DingZeZuo/Peking Union Medical College , China,0/128
  35. Clinical and Basic Studies in a Chinese Family with Paralysis Periodica Paramyotonia,FengZuo/China Medical University,0/47
  36. Clinical, Pathological and Genetic Study of Kennedy Disease in a Chinese Family,ZhaoMei/Second Military Medical University,0/92
  37. Molecular Epidemiology of Viral Diarrhea among Children in Shanghai,GongZhiXiang/Second Military Medical University,0/300
  38. Development of Techniques for Prenatal Genetic Diagnosis of Common Aneuploidy and Monogenic Diseases,LuYanPing/PLA Postgraduate Medical School,0/357
  39. Experimental Study on UbcH10 as a Marker for the Diagnosis and Therapy of Colorectal Cancer,ChenShiMin/Shandong University,0/137
  40. Systematic Review of Spinocerebellar Ataxias and Clinical Study of Spinocerebellar Ataxias in the Three Gorge Reservoir Area,HuangLiHua/Third Military Medical University,1/155
  41. Pedigrees of retinoblastoma gene mutation detection and genetic counseling,JiangWei/Peking Union Medical College , China,0/115
  42. Establishing a Genetic Diagnosis System for 46, XY DSD and Analyzing Gene Mutation for 46, XY Female /AIS/5α-RD2 Deficiency,LiaoXi/Central South University,0/27
  43. The Role of Nanobacteria in the Pathogenesis of Type Ⅲ Prostatitis and the Reseach of Specific Genetic Diagnosis,ShenXueCheng/Third Military Medical University,0/27
  44. The Establishment of Genetic Diagnosis Platform for Hereditary Cerebellar Ataxia and Mapping and Cloning of Novel Causative Genes for Hereditary Cerebellar Ataxia,WangJunLing/Central South University,0/222
  45. Polygenic Determinants of Parkinson’s Disease and the Establishment of Autosomal Dominant Parkinson’s Disease Genetic Diagnosis Platform,WangLei/Central South University,1/89
  46. FⅧ Gene Mutation Spectrum in Chinese Hemophilia A Patients,XueFeng/Peking Union Medical College , China,0/99
  47. Application of Fluorescence in Situ Hybridization in Assisted Reproductive Medicine,LiGang/Zhengzhou University,0/332
  48. Establishment and Application of Preimplantation Genetic Diagnostic Technique for Hereditary Hearing Loss and Study of Molecular Mechanism of Inherited Deafness Pedigrees,JinZhanGuo/PLA Postgraduate Medical School,0/50
  49. The Establishment of Long QT Interval Syndrome Gene Variants Database and the Screen of Gene Variants in Ten Chinese Families,ZhangTao/Zhejiang University,0/48
  50. Screening of GSTs-Mu Gene and COX Gene SNP Locus and Establishment the Method of Gene Diagnoses,ZhaoRuiFeng/Jilin University,0/80

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