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American Journal of Medical Genetics. Part A
|
November 28, 2014
Aortopathy in the 7q11.23 microduplication syndrome
Ashley Parrott, Jeanne James, Paula Goldenberg, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 2, 2019
Correction: Genetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)
Ray E Hershberger, Michael M Givertz, Carolyn Y Ho, et al.
Journal of Cardiac Failure
|
March 24, 2018
Genetic Evaluation of Cardiomyopathy-A Heart Failure Society of America Practice Guideline
Ray E Hershberger, Michael M Givertz, Carolyn Y Ho, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 16, 2018
Genetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)
Ray E Hershberger, Michael M Givertz, Carolyn Y Ho, et al.
Journal of Molecular and Cellular Cardiology Plus
|
July 18, 2025
Combined genome and transcriptome analysis identifies molecular signatures of aortic disease in patients with Marfan syndrome
Katherine B Stanley, Alexa V Mederos, Ethan H Barksdale, et al.
The Journal of Pediatrics
|
May 21, 2023
Genetic Testing Guidelines Impact Care in Newborns with Congenital Heart Defects
Matthew D Durbin, Korre Fairman, Lindsey R Helvaty, et al.
The Journal of Clinical Investigation
|
May 17, 2019
Imbalanced mitochondrial function provokes heterotaxy via aberrant ciliogenesis
Martin D Burkhalter, Arthi Sridhar, Pedro Sampaio, 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.
Journal of the American Heart Association
|
September 29, 2022
Learning to Crawl: Determining the Role of Genetic Abnormalities on Postoperative Outcomes in Congenital Heart Disease
Benjamin J Landis, Benjamin M Helm, Jeremy L Herrmann, et al.
HGG Advances
|
December 17, 2021
Identification of a common polymorphism in <i>COQ8B</i> acting as a modifier of thoracic aortic aneurysm severity
Benjamin J Landis, Dongbing Lai, Dong-Chuan Guo, et al.
Page
of 15
Search research articles
Search
Showing results (101-110 of 146) with videos related to
Sort By:
Page
of 15
American Journal of Medical Genetics. Part A
|
November 28, 2014
Aortopathy in the 7q11.23 microduplication syndrome
Ashley Parrott, Jeanne James, Paula Goldenberg, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 2, 2019
Correction: Genetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)
Ray E Hershberger, Michael M Givertz, Carolyn Y Ho, et al.
Journal of Cardiac Failure
|
March 24, 2018
Genetic Evaluation of Cardiomyopathy-A Heart Failure Society of America Practice Guideline
Ray E Hershberger, Michael M Givertz, Carolyn Y Ho, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 16, 2018
Genetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)
Ray E Hershberger, Michael M Givertz, Carolyn Y Ho, et al.
Journal of Molecular and Cellular Cardiology Plus
|
July 18, 2025
Combined genome and transcriptome analysis identifies molecular signatures of aortic disease in patients with Marfan syndrome
Katherine B Stanley, Alexa V Mederos, Ethan H Barksdale, et al.
The Journal of Pediatrics
|
May 21, 2023
Genetic Testing Guidelines Impact Care in Newborns with Congenital Heart Defects
Matthew D Durbin, Korre Fairman, Lindsey R Helvaty, et al.
The Journal of Clinical Investigation
|
May 17, 2019
Imbalanced mitochondrial function provokes heterotaxy via aberrant ciliogenesis
Martin D Burkhalter, Arthi Sridhar, Pedro Sampaio, 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.
Journal of the American Heart Association
|
September 29, 2022
Learning to Crawl: Determining the Role of Genetic Abnormalities on Postoperative Outcomes in Congenital Heart Disease
Benjamin J Landis, Benjamin M Helm, Jeremy L Herrmann, et al.
HGG Advances
|
December 17, 2021
Identification of a common polymorphism in <i>COQ8B</i> acting as a modifier of thoracic aortic aneurysm severity
Benjamin J Landis, Dongbing Lai, Dong-Chuan Guo, et al.
Page
of 15