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Pediatric Cardiology
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December 1, 2017
Genetic Testing in Pediatric Cardiomyopathy
Chalani D Ellepola, Linda M Knight, Peter Fischbach, et al.
Journal of Genetic Counseling
|
November 1, 2024
Genetic testing and counseling for hypertrophic cardiomyopathy: An evidence-based practice resource of the National Society of Genetic Counselors
Erin M Miller, Emily Brown, Susan Christian, et al.
Heart Rhythm
|
June 24, 2019
Genetic testing and cascade screening in pediatric long QT syndrome and hypertrophic cardiomyopathy
Linda M Knight, Erin Miller, Joshua Kovach, et al.
The Biochemical Journal
|
July 26, 2023
RyR2 C-terminal truncating variants identified in patients with arrhythmic phenotypes exert a dominant negative effect through formation of wildtype-truncation heteromers
Shanshan Tian, Xiaowei Zhong, Hui Wang, et al.
Circulation
|
July 23, 2020
An International Multicenter Evaluation of Inheritance Patterns, Arrhythmic Risks, and Underlying Mechanisms of <i>CASQ2</i>-Catecholaminergic Polymorphic Ventricular Tachycardia
Kevin Ng, Erron W Titus, Krystien V Lieve, et al.
Circulation
|
January 17, 2020
An International Multicenter Evaluation of Type 5 Long QT Syndrome: A Low Penetrant Primary Arrhythmic Condition
Jason D Roberts, S Yukiko Asaki, Andrea Mazzanti, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 6) with videos related to
Sort By:
Page
of 1
Pediatric Cardiology
|
December 1, 2017
Genetic Testing in Pediatric Cardiomyopathy
Chalani D Ellepola, Linda M Knight, Peter Fischbach, et al.
Journal of Genetic Counseling
|
November 1, 2024
Genetic testing and counseling for hypertrophic cardiomyopathy: An evidence-based practice resource of the National Society of Genetic Counselors
Erin M Miller, Emily Brown, Susan Christian, et al.
Heart Rhythm
|
June 24, 2019
Genetic testing and cascade screening in pediatric long QT syndrome and hypertrophic cardiomyopathy
Linda M Knight, Erin Miller, Joshua Kovach, et al.
The Biochemical Journal
|
July 26, 2023
RyR2 C-terminal truncating variants identified in patients with arrhythmic phenotypes exert a dominant negative effect through formation of wildtype-truncation heteromers
Shanshan Tian, Xiaowei Zhong, Hui Wang, et al.
Circulation
|
July 23, 2020
An International Multicenter Evaluation of Inheritance Patterns, Arrhythmic Risks, and Underlying Mechanisms of <i>CASQ2</i>-Catecholaminergic Polymorphic Ventricular Tachycardia
Kevin Ng, Erron W Titus, Krystien V Lieve, et al.
Circulation
|
January 17, 2020
An International Multicenter Evaluation of Type 5 Long QT Syndrome: A Low Penetrant Primary Arrhythmic Condition
Jason D Roberts, S Yukiko Asaki, Andrea Mazzanti, et al.
Page
of 1