75 results on '"Jun, C"'
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2. Hemorrhagic Stroke and the Japan Adult Moyamoya Trial
3. Next Generation Sequencing (NGS) Based Panel Analysis of Metabolic Pathways
4. Overview of the Clinical Utility of Next Generation Sequencing in Molecular Diagnoses of Human Genetic Disorders
5. Detection of Copy Number Variations (CNVs) Based on the Coverage Depth from the Next Generation Sequencing Data
6. Comprehensive Analyses of the Mitochondrial Genome
7. A New Economical Method for Fabricating High-Purity Bi2O3 via Extraction-Precipitation Stripping and Post Annealing
8. A Novel Preparation of Bi2O3 and Their Potent Photocatalytic Activity Under Visible-Light Irradiation
9. Multimodal Interventional Treatment and Outcomes for Unruptured Arteriovenous Malformations
10. Moyamoya Disease (Spontaneous Occlusion of the Circle of Willis)
11. Hereditary Paraganglioma and Pheochromocytoma
12. Frequently Asked Questions About the Clinical Utility of Next-Generation Sequencing in Molecular Diagnosis of Human Genetic Diseases
13. Validation of NGS-Based DNA Testing and Implementation of Quality Control Procedures
14. Next-Generation Sequencing Analyses of the Whole Mitochondrial Genome
15. Clinical Molecular Diagnostic Techniques: A Brief Review
16. Mitochondrial Respiratory Chain Complex II
17. Biochemical and Molecular Methods for the Study of Mitochondrial Disorders
18. Application of Next Generation Sequencing to Molecular Diagnosis of Inherited Diseases
19. Moyamoya Disease in Adult: Management of Hemorrhage
20. Pregnancy and Delivery in Moyamoya Disease
21. Somatic Mitochondrial DNA Mutations in Oral Cancer of Betel Quid Chewers
22. Quantitative PCR Analysis of Mitochondrial DNA Content in Patients with Mitochondrial Disease
23. Enhanced Detection of Deleterious Mutations by TTGE Analysis of Mother and Child’s DNA Side by Side
24. Comprehensive Molecular Diagnosis of Mitochondrial Disorders : Qualitative and Quantitative Approach
25. Subretinal Iodoacetate : A Model of Retinal Degeneration in Cats
26. Development of Finish Turning Inserts: Present Trends and Future Prospects
27. Next Generation Sequencing Based Clinical Molecular Diagnosis of Human Genetic Disorders
28. Next Generation Sequencing : Translation to Clinical Diagnostics
29. Mitochondrial Disorders Caused by Nuclear Genes
30. Application of Next-Generation Sequencing to Hearing Loss
31. Next-Generation Sequencing Based Clinical Molecular Diagnosis of Primary Immunodeficiency Diseases
32. Application of Next-Generation Sequencing in Noonan Spectrum Disorders
33. Diagnosing Hereditary Cancer Susceptibility Through Multigene Panel Testing
34. Next-Generation Sequencing Based Testing for Disorders of the Skeleton
35. The Next Generation Sequencing Based Molecular Diagnosis of Visual Diseases
36. Next Generation of Carrier Screening
37. Exome Sequencing in the Clinical Setting
38. Family-Based Next-Generation Sequencing Analysis
39. Application of NGS in the Diagnosis of Cardiovascular Genetic Diseases
40. Next-Generation Sequencing for the Diagnosis of Monogenic Disorders of Insulin Secretion
41. The Applications and Challenges of Next-Generation Sequencing in Diagnosing Neuromuscular Disorders
42. NGS Improves the Diagnosis of X-Linked Intellectual Disability (XLID)
43. Guidelines and Approaches to Compliance with Regulatory and Clinical Standards: Quality Control Procedures and Quality Assurance
44. Molecular Diagnosis of Congenital Disorders of Glycosylation (CDG)
45. Sequence Alignment, Analysis, and Bioinformatic Pipelines
46. Methods of Gene Enrichment and Massively Parallel Sequencing Technologies
47. Noninvasive Prenatal Diagnosis Using Next-Generation Sequencing
48. NGS-Based Clinical Diagnosis of Genetically Heterogeneous Disorders
49. Application of Next-Generation Sequencing of Nuclear Genes for Mitochondrial Disorders
50. NGS Analysis of Heterogeneous Retinitis Pigmentosa
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