289 results on '"Kumar, Dhavendra"'
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2. Contributors
3. Preface
4. Global perspectives of genomic education and training
5. Introduction to Genes, Genome and Inheritance
6. Indigenous population genome databases for India and South Asia: emerging need for health and social applications
7. Quantifying the contribution of recessive coding variation to developmental disorders
8. Preface
9. Familial hypercholesterolaemia
10. Congenital heart disease
11. Hereditary haemorrhagic telangiectasia
12. Metabolic disease and neuromuscular disorders
13. Genes, genome, and inheritance patterns
14. Coronary artery disease and myocardial infarction
15. Inherited arrhythmias and conduction disorders
16. Pulmonary arterial hypertension
17. Marfan syndrome and related inherited disorders of connective tissue
18. Mitochondrial cardiovascular diseases
19. Introduction
20. The heart and inherited haematological disorders
21. Genetic counselling
22. Cardiomyopathies
23. Genetic laboratory techniques
24. Stroke
25. Molecular biology of acute and chronic inflammation
26. Glossary—molecular medicine
27. About the author
28. Preface
29. Molecular medicine of diabetes mellitus
30. List of contributors
31. Gene, genome, and molecular therapeutics
32. The human genome and molecular medicine
33. Integrated genomic and molecular medicine
34. Preface: The origin of life and astrobiology
35. Acknowledgement and Disclaimer
36. Chapter 1 - Introduction to genomic and molecular biology
37. Chapter 20 - Cardiovascular precision and personalised medicine
38. Chapter 16 - Genetic and metabolic perspectives of heart failure
39. Preface
40. From the double helix to the personal genomes
41. The genomic health care in modern medicine
42. Genetic Counselling for Families from the Indian Subcontinent
43. Congenital Developmental Anomalies
44. Diabetes Mellitus and Related Disorders
45. The Genetics of Cancer: The Indian Subcontinent Perspective
46. Inherited Skeletal Dysplasias and Collagen Diseases
47. Genetic Neurological and Psychiatric Diseases
48. The Indian Subcontinent and Human Genetics: An Introduction
49. Epidemiology of Genetic Diseases
50. Heterozygous mutations affecting the protein kinase domain of CDK13 cause a syndromic form of developmental delay and intellectual disability
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