Dissertation 

About 17 item dissertation in line with denaturing high performance liquid chromatography (DHPLC) query results,the following is 1 to 50(Search took 0.039 seconds)

  1. Cloning and Expression of the F1L Gene of CEV and Establishment and Preliminary Application of Molecular Biological Detection Methods,ShaoHongZe/Jilin Agricultural University,0/39
  2. The Prevalence of BRCA1 and BRCA2 Germline Mutations in High-Risk Breast Cancer Patients of Chinese Han Nationality,LiWenFeng/Fudan University,2/365
  3. 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
  4. Clinical and Experimental Research of Tuberous Sclerosis,SunXinFen/Fudan University,0/149
  5. Analysis of Mitochondrial DNA Polymorphisms Based on Denaturing High-Performance Liquid Chromatography and Its Study in Forensic Application,WangXuDong/Sichuan University,0/268
  6. Nasopharyngeal Carcinoma Related Genes and Their Single Nucleotide Polymorphisms Screened out from 6p21.3,HuangHua/First Military Medical University,0/91
  7. Study on Association of TGFBR3 Gene Polymorphism with Idiopathic Premature Ovarian Failure,ZuoChunRong/Southern Medical University,,0/64
  8. The Studies and Application of Gene Diagnosis for Spinal Muscular Atrophy,RenMeiHong/China Medical University,0/63
  9. Rapid Genotyping of Known Mutations and Polymorphisms in Beta-globin Gene Based on the DHPLC Profile Patterns of Homoduplexes and Heteroduplexes,LiQiang/First Military Medical University,0/135
  10. Study on Characteristics of Mutation of Senataxin Gene in Amyotrophic Lateral Sclerosis,ChenWenZu/Fujian Medical,0/35
  11. Detect MFN2 Gene Mutation by Using Denaturing High Performance Liquid Chromatography,FuMin/Central South University,0/125
  12. Association of Serum Matrix Metallproteinase-2、3、9 Concerntration and Gene Polymorphism to Atherosclerotic Cerebral Infarction,LiuZuoJie/Yangzhou University,1/217
  13. Screening and Analysis of Fibrillin-1 Gene (FBN1) Mutation in a Chinese Family with Isolated Ectopia Lentis and Association Study of Schizophrenia and the Polymorphisms of COMT Gene in a Chinese Han Population,YuZuo/Shanghai Institutes for Biological Sciences,0/62
  14. Study on the Gene Diagnosis and the Genotype-Phenotype Correlation of Spinal Muscular Atrophy,ChenWanJin/Fujian Medical,0/74
  15. Molecular Characterization of SMN1 Copy Number in the Chinese Population and Rapid Genotyping of Spinal Muscular Atrophy Determinants,ZhuShengYuan/Southern Medical University,,0/62
  16. Deletion Duchenne muscular dystrophy and carrier detection system improvement and its application,ChenZhiTing/Fujian Medical,1/47
  17. Using SNPS Sites on the Non-Invasive Prenatal Diagnosis of Down’s Syndrome,WeiXiaoJing/Shanxi Medical,0/54

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