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Gretchen MacCarrick

Showing results (31-40 of 38) with videos related to

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European Journal of Human Genetics : EJHG|February 24, 2019
Confirmation of the role of pathogenic SMAD6 variants in bicuspid aortic valve-related aortopathyIlse Luyckx, Gretchen MacCarrick, Marlies Kempers, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|March 18, 2025
Family functioning and health-related quality of life in children and young adults with Marfan syndromeLauren S Crafts, Lynn A Sleeper, Karen Uzark, et al.
Clinical Trials (London, England)|August 22, 2020
Recruitment, retention, and adherence in a clinical trial: The Pediatric Heart Network's Marfan Trial experienceMichelle S Hamstra, Victoria L Pemberton, Nicholas Dagincourt, et al.
Medrxiv : the Preprint Server for Health Sciences|November 19, 2025
Cardiovascular genetic counseling is associated with improved patient-reported outcomes across clinical indications and settingsBrittney Murray, Catherine Gordon, Susan Christian, et al.
Human Mutation|February 3, 2018
A mutation update on the LDS-associated genes TGFB2/3 and SMAD2/3Dorien Schepers, Giada Tortora, Hiroko Morisaki, et al.
Nature Genetics|November 21, 2018
ROBO4 variants predispose individuals to bicuspid aortic valve and thoracic aortic aneurysmRussell A Gould, Hamza Aziz, Courtney E Woods, et al.
American Journal of Human Genetics|March 13, 2025
Bi-allelic MED16 variants cause a MEDopathy with intellectual disability, motor delay, and craniofacial, cardiac, and limb malformationsCharlotte Guillouet, Valeria Agostini, Geneviève Baujat, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 16, 2026
Loeys-Dietz Syndrome: 2026 updated care management primerGretchen MacCarrick, Rana O Afifi, Rebecca Allen, et al.
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Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
European Journal of Human Genetics : EJHG|February 24, 2019
Confirmation of the role of pathogenic SMAD6 variants in bicuspid aortic valve-related aortopathyIlse Luyckx, Gretchen MacCarrick, Marlies Kempers, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|March 18, 2025
Family functioning and health-related quality of life in children and young adults with Marfan syndromeLauren S Crafts, Lynn A Sleeper, Karen Uzark, et al.
Clinical Trials (London, England)|August 22, 2020
Recruitment, retention, and adherence in a clinical trial: The Pediatric Heart Network's Marfan Trial experienceMichelle S Hamstra, Victoria L Pemberton, Nicholas Dagincourt, et al.
Medrxiv : the Preprint Server for Health Sciences|November 19, 2025
Cardiovascular genetic counseling is associated with improved patient-reported outcomes across clinical indications and settingsBrittney Murray, Catherine Gordon, Susan Christian, et al.
Human Mutation|February 3, 2018
A mutation update on the LDS-associated genes TGFB2/3 and SMAD2/3Dorien Schepers, Giada Tortora, Hiroko Morisaki, et al.
Nature Genetics|November 21, 2018
ROBO4 variants predispose individuals to bicuspid aortic valve and thoracic aortic aneurysmRussell A Gould, Hamza Aziz, Courtney E Woods, et al.
American Journal of Human Genetics|March 13, 2025
Bi-allelic MED16 variants cause a MEDopathy with intellectual disability, motor delay, and craniofacial, cardiac, and limb malformationsCharlotte Guillouet, Valeria Agostini, Geneviève Baujat, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 16, 2026
Loeys-Dietz Syndrome: 2026 updated care management primerGretchen MacCarrick, Rana O Afifi, Rebecca Allen, et al.
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