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Journal of Community Genetics
|
August 13, 2021
Psychological distress in response to physical activity restrictions in patients with non-syndromic thoracic aortic aneurysm/dissection
Alexis McEntire, Benjamin M Helm, Benjamin J Landis, et al.
Congenital Heart Disease
|
June 21, 2013
Genetic testing practices in infants with congenital heart disease
Jessica 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 Services
Benjamin 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 defects
Aaliya 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 bullosa
Thomas 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 Disease
Jacqueline 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 genes
Helen 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 risk
Christopher 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 heterotaxy
John R Wells, Maria B Padua, Allison M Haaning, et al.
Human Molecular Genetics
|
May 9, 2023
Congenital heart defects caused by FOXJ1
Maria B Padua, Benjamin M Helm, John R Wells, et al.
Page
of 15
Search research articles
Search
Showing results (71-80 of 146) with videos related to
Sort By:
Page
of 15
Journal of Community Genetics
|
August 13, 2021
Psychological distress in response to physical activity restrictions in patients with non-syndromic thoracic aortic aneurysm/dissection
Alexis McEntire, Benjamin M Helm, Benjamin J Landis, et al.
Congenital Heart Disease
|
June 21, 2013
Genetic testing practices in infants with congenital heart disease
Jessica 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 Services
Benjamin 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 defects
Aaliya 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 bullosa
Thomas 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 Disease
Jacqueline 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 genes
Helen 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 risk
Christopher 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 heterotaxy
John R Wells, Maria B Padua, Allison M Haaning, et al.
Human Molecular Genetics
|
May 9, 2023
Congenital heart defects caused by FOXJ1
Maria B Padua, Benjamin M Helm, John R Wells, et al.
Page
of 15