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JACC. Basic to Translational Science
|
April 10, 2023
Cardiac Transcriptome Remodeling and Impaired Bioenergetics in Single-Ventricle Congenital Heart Disease
Anastacia M Garcia, Lee S Toni, Carissa A Miyano, et al.
Circulation. Genomic and Precision Medicine
|
July 13, 2021
Impact of Genetic Testing for Cardiomyopathy on Emotional Well-Being and Family Dynamics: A Study of Parents and Adolescents
Priyanka Ahimaz, Maya Sabatello, Min Qian, et al.
Science (New York, N.Y.)
|
November 10, 1995
Genomic structure of an attenuated quasi species of HIV-1 from a blood transfusion donor and recipients
N J Deacon, A Tsykin, A Solomon, et al.
American Journal of Medical Genetics. Part A
|
June 22, 2019
Costello syndrome: Clinical phenotype, genotype, and management guidelines
Karen W Gripp, Lindsey A Morse, Marni Axelrad, et al.
Human Molecular Genetics
|
June 23, 2018
Biallelic B3GALT6 mutations cause spondylodysplastic Ehlers-Danlos syndrome
Tim Van Damme, Xiaomeng Pang, Brecht Guillemyn, et al.
Mitochondrion
|
May 26, 2024
ACAD9 treatment with bezafibrate and nicotinamide riboside temporarily stabilizes cardiomyopathy and lactic acidosis
Johan L K Van Hove, Marisa W Friederich, Daniella H Hock, et al.
Stem Cell Reports
|
February 26, 2021
Maturation of Pluripotent Stem Cell-Derived Cardiomyocytes Enables Modeling of Human Hypertrophic Cardiomyopathy
Walter E Knight, Yingqiong Cao, Ying-Hsi Lin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 5, 2018
Clinical history and management recommendations of the smooth muscle dysfunction syndrome due to ACTA2 arginine 179 alterations
Ellen S Regalado, Lauren Mellor-Crummey, Julie De Backer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 2, 2020
Automated syndrome diagnosis by three-dimensional facial imaging
Benedikt Hallgrímsson, J David Aponte, David C Katz, et al.
Nature Communications
|
October 5, 2018
Pathogenic variants in glutamyl-tRNA<sup>Gln</sup> amidotransferase subunits cause a lethal mitochondrial cardiomyopathy disorder
Marisa W Friederich, Sharita Timal, Christopher A Powell, et al.
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Showing results (51-60 of 60) with videos related to
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Page
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You have reached the last page of results.
This site can display upto 60 results.
JACC. Basic to Translational Science
|
April 10, 2023
Cardiac Transcriptome Remodeling and Impaired Bioenergetics in Single-Ventricle Congenital Heart Disease
Anastacia M Garcia, Lee S Toni, Carissa A Miyano, et al.
Circulation. Genomic and Precision Medicine
|
July 13, 2021
Impact of Genetic Testing for Cardiomyopathy on Emotional Well-Being and Family Dynamics: A Study of Parents and Adolescents
Priyanka Ahimaz, Maya Sabatello, Min Qian, et al.
Science (New York, N.Y.)
|
November 10, 1995
Genomic structure of an attenuated quasi species of HIV-1 from a blood transfusion donor and recipients
N J Deacon, A Tsykin, A Solomon, et al.
American Journal of Medical Genetics. Part A
|
June 22, 2019
Costello syndrome: Clinical phenotype, genotype, and management guidelines
Karen W Gripp, Lindsey A Morse, Marni Axelrad, et al.
Human Molecular Genetics
|
June 23, 2018
Biallelic B3GALT6 mutations cause spondylodysplastic Ehlers-Danlos syndrome
Tim Van Damme, Xiaomeng Pang, Brecht Guillemyn, et al.
Mitochondrion
|
May 26, 2024
ACAD9 treatment with bezafibrate and nicotinamide riboside temporarily stabilizes cardiomyopathy and lactic acidosis
Johan L K Van Hove, Marisa W Friederich, Daniella H Hock, et al.
Stem Cell Reports
|
February 26, 2021
Maturation of Pluripotent Stem Cell-Derived Cardiomyocytes Enables Modeling of Human Hypertrophic Cardiomyopathy
Walter E Knight, Yingqiong Cao, Ying-Hsi Lin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 5, 2018
Clinical history and management recommendations of the smooth muscle dysfunction syndrome due to ACTA2 arginine 179 alterations
Ellen S Regalado, Lauren Mellor-Crummey, Julie De Backer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 2, 2020
Automated syndrome diagnosis by three-dimensional facial imaging
Benedikt Hallgrímsson, J David Aponte, David C Katz, et al.
Nature Communications
|
October 5, 2018
Pathogenic variants in glutamyl-tRNA<sup>Gln</sup> amidotransferase subunits cause a lethal mitochondrial cardiomyopathy disorder
Marisa W Friederich, Sharita Timal, Christopher A Powell, et al.
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of 6