Search research articles
Contact Us
Filters
Showing results (31-40 of 89) with videos related to
Page
of 9
Sort By:
Nature Cardiovascular Research
|
April 26, 2024
Exploring the complex spectrum of dominance and recessiveness in genetic cardiomyopathies
Alex Lipov, Sean J Jurgens, Francesco Mazzarotto, et al.
Global Cardiology Science & Practice
|
November 5, 2015
Genetic modifiers to the PLN L39X mutation in a patient with DCM and sustained ventricular tachycardia?
Despina Sanoudou, Fotis Kolokathis, Demetris Arvanitis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 19, 2017
Using high-resolution variant frequencies to empower clinical genome interpretation
Nicola Whiffin, Eric Minikel, Roddy Walsh, et al.
Pulmonary Pharmacology & Therapeutics
|
April 15, 2008
Anti-inflammatory modulation of chronic airway inflammation in the murine house dust mite model
Kristina Ulrich, Jennifer S Hincks, Roddy Walsh, et al.
Plos One
|
July 18, 2013
Towards clinical molecular diagnosis of inherited cardiac conditions: a comparison of bench-top genome DNA sequencers
Xinzhong Li, Andrew J Buckton, Samuel L Wilkinson, et al.
Clinical Science (London, England : 1979)
|
November 26, 2013
Detection of mutations in KLHL3 and CUL3 in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome)
Mark Glover, James S Ware, Amanda Henry, et al.
Circulation
|
April 29, 2021
Variant Intronic Enhancer Controls <i>SCN10A-short</i> Expression and Heart Conduction
Joyce C K Man, Fernanda M Bosada, Koen T Scholman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 8, 2018
Defining the diagnostic effectiveness of genes for inclusion in panels: the experience of two decades of genetic testing for hypertrophic cardiomyopathy at a single center
Francesco Mazzarotto, Francesca Girolami, Beatrice Boschi, et al.
European Heart Journal
|
November 18, 2025
Automated patch clamp data improve variant classification and penetrance stratification for SCN5A-Brugada syndrome
Matthew J O'Neill, Joanne G Ma, Jessa L Aldridge, et al.
Cardiovascular Research
|
May 26, 2018
Complex roads from genotype to phenotype in dilated cardiomyopathy: scientific update from the Working Group of Myocardial Function of the European Society of Cardiology
Antoine Bondue, Eloisa Arbustini, Anna Bianco, et al.
Page
of 9
Search research articles
Search
Showing results (31-40 of 89) with videos related to
Sort By:
Page
of 9
Nature Cardiovascular Research
|
April 26, 2024
Exploring the complex spectrum of dominance and recessiveness in genetic cardiomyopathies
Alex Lipov, Sean J Jurgens, Francesco Mazzarotto, et al.
Global Cardiology Science & Practice
|
November 5, 2015
Genetic modifiers to the PLN L39X mutation in a patient with DCM and sustained ventricular tachycardia?
Despina Sanoudou, Fotis Kolokathis, Demetris Arvanitis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 19, 2017
Using high-resolution variant frequencies to empower clinical genome interpretation
Nicola Whiffin, Eric Minikel, Roddy Walsh, et al.
Pulmonary Pharmacology & Therapeutics
|
April 15, 2008
Anti-inflammatory modulation of chronic airway inflammation in the murine house dust mite model
Kristina Ulrich, Jennifer S Hincks, Roddy Walsh, et al.
Plos One
|
July 18, 2013
Towards clinical molecular diagnosis of inherited cardiac conditions: a comparison of bench-top genome DNA sequencers
Xinzhong Li, Andrew J Buckton, Samuel L Wilkinson, et al.
Clinical Science (London, England : 1979)
|
November 26, 2013
Detection of mutations in KLHL3 and CUL3 in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome)
Mark Glover, James S Ware, Amanda Henry, et al.
Circulation
|
April 29, 2021
Variant Intronic Enhancer Controls <i>SCN10A-short</i> Expression and Heart Conduction
Joyce C K Man, Fernanda M Bosada, Koen T Scholman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 8, 2018
Defining the diagnostic effectiveness of genes for inclusion in panels: the experience of two decades of genetic testing for hypertrophic cardiomyopathy at a single center
Francesco Mazzarotto, Francesca Girolami, Beatrice Boschi, et al.
European Heart Journal
|
November 18, 2025
Automated patch clamp data improve variant classification and penetrance stratification for SCN5A-Brugada syndrome
Matthew J O'Neill, Joanne G Ma, Jessa L Aldridge, et al.
Cardiovascular Research
|
May 26, 2018
Complex roads from genotype to phenotype in dilated cardiomyopathy: scientific update from the Working Group of Myocardial Function of the European Society of Cardiology
Antoine Bondue, Eloisa Arbustini, Anna Bianco, et al.
Page
of 9