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21. With Hbsag Positive Asymptomatic Blood Donors And Chronic Active Hepatitis Patients With Hepatitis B Virus Pre-c Gene Mutation
22. Preliminary Research On DNA Methylation Of Paternal And Maternal Imprinted Gene In Sperm Of Infertile Males
23. A Study On The Mutations Of MT-2A Gene In The Tissues Of Squamous Cell Carcinoma Of The Esophagus By Direct Sequencing Test
24. Application Of Combining Direct Sequencing And CNV Detection Technology In Waardenburg Syndrome-related Genes Screening
25. Association Of C5L2and C5aR1 Genetic Polymorphisms Genetic Polymorphisms With Pathogenesis And Prognosis Of Coronary Artery Disease
26. Clinicopathologic And Molecularpathologic Study Of Tumors Associated With Deficient INI1,a Core Subunit Of SWI/SNF Complex
27. Diagnosis Of Patients With Tuberous Sclerosis Complex By Direct Sequencing And MLPA
28. A Study On The Mutations Of BRAF Gene In The Tissues Of Non-small Cell Lung Cancer
29. Study Of Gene Mutations And Genotyping Of Hepatitis B Virus By PCR-reverse Dot Blot And PCR-direct DNA Sequencing
30. Mutation Analysis Of The TSC1and TSC2Genes In Chinese Patients With Tuberous Sclerosis Complex
31. The Experimental Study On Detection Of K-ras Mutation Through PNA-clamp Mediated Real-time PCR In Colorectal Cancer
32. K-ras Gene Mutation Relationship With The Biological Behavior Of Colorectal Cancer Correlation Analysis And Adverse Reactions With FOLFOX
33. P16 Expression And The C-Kit Gene Mutation Of The Small Gastrointestinal Stromal Tumor In Stomach
34. Clinical Detecting Methodology Comparison And Influence Factors Analysis Of EGFR And KRAS Gene Mutation
35. Research On Relations Between Polymorphism Of HLA-DQ Gene Rs9275319 And Hepatitis B-related Liver Cancer
36. Clinical Evaluation Of An Improved Method For Epidermal Growth Factor Receptor Mutation Detection
37. The Population Genetics Research Of Drug Metabolic Enzymes CYP2S1,CYP2R1 And CYP2J2 In Diffferent Chinese Populations
38. Mutation Screening In Families With Two Rare Diseases By Candidate Gene Approach
39. The role of WNT10A in familial tooth agenesis
40. Polygenic Determinants Of Parkinson's Disease And The Establishment Of Autosomal Dominant Parkinson's Disease Genetic Diagnosis Platform
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