27 results on '"Mates, Jesus"'
Search Results
2. Sudden Cardiac Death and Copy Number Variants: What Do We Know after 10 Years of Genetic Analysis?
3. Molecular autopsy in a cohort of infants died suddenly at rest
4. Genetic analysis in post-mortem samples with micro-ischemic alterations
5. A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia
6. Sudden Arrhythmic Death During Exercise: A Post-Mortem Genetic Analysis
7. Post-mortem genetic analysis in juvenile cases of sudden cardiac death
8. The role of clinical, genetic and segregation evaluation in sudden infant death
9. Genetic investigation of sudden unexpected death in epilepsy cohort by panel target resequencing
10. Short QT Syndrome: A Comprehensive Genetic Interpretation and Clinical Translation of Rare Variants
11. Personalized Interpretation and Clinical Translation of Genetic Variants Associated With Cardiomyopathies
12. Genetic interpretation and clinical translation of minor genes related to Brugada syndrome
13. Role of genetic and electrolyte abnormalities in prolonged QTc interval and sudden cardiac death in end-stage renal disease patients
14. Role of copy number variants in sudden cardiac death and related diseases: genetic analysis and translation into clinical practice
15. Incomplete Penetrance and Variable Expressivity: Hallmarks in Channelopathies Associated with Sudden Cardiac Death
16. Additional value of screening for minor genes and copy number variants in hypertrophic cardiomyopathy
17. Correction: Natural and Undetermined Sudden Death: Value of Post-Mortem Genetic Investigation
18. Natural and Undetermined Sudden Death: Value of Post-Mortem Genetic Investigation
19. Large Genomic Imbalances in Brugada Syndrome
20. Regulome‐Seq: Searching for Single Nucleotide Variants (SNVs) Associated with Disease Beyond Protein‐Coding Regions
21. A Genetically Vulnerable Myocardium May Predispose to Myocarditis
22. Rare Titin (TTN) Variants in Diseases Associated with Sudden Cardiac Death
23. Incomplete Penetrance and Variable Expressivity: Hallmarks in Channelopathies Associated with Sudden Cardiac Death.
24. Genetic investigation of sudden unexpected death in epilepsy cohort by panel target resequencing
25. Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome
26. Next Generation Sequencing: The Current Challenge is the Translation into Clinics
27. Identification of Genetic Alterations, as Causative Genetic Defects in Long QT Syndrome, Using Next Generation Sequencing Technology
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