Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Stephanie M Ware

Showing results (71-80 of 146) with videos related to

Pageof 15
Sort By:
Journal of Community Genetics|August 13, 2021
Psychological distress in response to physical activity restrictions in patients with non-syndromic thoracic aortic aneurysm/dissectionAlexis McEntire, Benjamin M Helm, Benjamin J Landis, et al.
Congenital Heart Disease|June 21, 2013
Genetic testing practices in infants with congenital heart diseaseJessica A Connor, Robert B Hinton, Erin M Miller, et al.
Journal of Genetic Counseling|October 29, 2017
The Genetic Counselor in the Pediatric Arrhythmia Clinic: Review and Assessment of ServicesBenjamin M Helm, Samantha L Freeze, Katherine G Spoonamore, et al.
Journal of Genetic Counseling|December 8, 2021
Assessing genetic counselors' graduate school education and training in congenital heart defectsAaliya Ahmad, Sara M Fitzgerald-Butt, Stephanie M Ware, et al.
Circulation. Heart Failure|September 20, 2012
Left ventricular noncompaction cardiomyopathy and aortopathy in a patient with recessive dystrophic epidermolysis bullosaThomas D Ryan, Stephanie M Ware, Anne W Lucky, et al.
Journal of the American Heart Association|March 13, 2025
Identification of Long Noncoding RNA Candidate Disease Genes Associated With Clinically Reported Copy Number Variants in Congenital Heart DiseaseJacqueline S Penaloza, Blythe Moreland, Jeffrey B Gaither, et al.
Scientific Reports|July 1, 2023
Single cell RNA analysis of the left-right organizer transcriptome reveals potential novel heterotaxy genesHelen M Bellchambers, Amruta R Phatak, Mardi J Nenni, et al.
Cardiology in the Young|January 28, 2020
Adolescents with congenital heart defects: a patient and parental perspective of genetic information and genetic riskChristopher A Crawford, Courtney E Vujakovich, Lindsey Elmore, et al.
HGG Advances|September 14, 2024
Non-coding cause of congenital heart defects: Abnormal RNA splicing with multiple isoforms as a mechanism for heterotaxyJohn R Wells, Maria B Padua, Allison M Haaning, et al.
Human Molecular Genetics|May 9, 2023
Congenital heart defects caused by FOXJ1Maria B Padua, Benjamin M Helm, John R Wells, et al.
Pageof 15

Showing results (71-80 of 146) with videos related to

Sort By:
Pageof 15
Journal of Community Genetics|August 13, 2021
Psychological distress in response to physical activity restrictions in patients with non-syndromic thoracic aortic aneurysm/dissectionAlexis McEntire, Benjamin M Helm, Benjamin J Landis, et al.
Congenital Heart Disease|June 21, 2013
Genetic testing practices in infants with congenital heart diseaseJessica A Connor, Robert B Hinton, Erin M Miller, et al.
Journal of Genetic Counseling|October 29, 2017
The Genetic Counselor in the Pediatric Arrhythmia Clinic: Review and Assessment of ServicesBenjamin M Helm, Samantha L Freeze, Katherine G Spoonamore, et al.
Journal of Genetic Counseling|December 8, 2021
Assessing genetic counselors' graduate school education and training in congenital heart defectsAaliya Ahmad, Sara M Fitzgerald-Butt, Stephanie M Ware, et al.
Circulation. Heart Failure|September 20, 2012
Left ventricular noncompaction cardiomyopathy and aortopathy in a patient with recessive dystrophic epidermolysis bullosaThomas D Ryan, Stephanie M Ware, Anne W Lucky, et al.
Journal of the American Heart Association|March 13, 2025
Identification of Long Noncoding RNA Candidate Disease Genes Associated With Clinically Reported Copy Number Variants in Congenital Heart DiseaseJacqueline S Penaloza, Blythe Moreland, Jeffrey B Gaither, et al.
Scientific Reports|July 1, 2023
Single cell RNA analysis of the left-right organizer transcriptome reveals potential novel heterotaxy genesHelen M Bellchambers, Amruta R Phatak, Mardi J Nenni, et al.
Cardiology in the Young|January 28, 2020
Adolescents with congenital heart defects: a patient and parental perspective of genetic information and genetic riskChristopher A Crawford, Courtney E Vujakovich, Lindsey Elmore, et al.
HGG Advances|September 14, 2024
Non-coding cause of congenital heart defects: Abnormal RNA splicing with multiple isoforms as a mechanism for heterotaxyJohn R Wells, Maria B Padua, Allison M Haaning, et al.
Human Molecular Genetics|May 9, 2023
Congenital heart defects caused by FOXJ1Maria B Padua, Benjamin M Helm, John R Wells, et al.
Pageof 15