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The Journal of Clinical Investigation
|
July 30, 2024
Early ascertainment of genetic diagnoses clarifies impact on medium-term survival following neonatal congenital heart surgery
Benjamin J Landis, Benjamin M Helm, Matthew D Durbin, et al.
Molecular Genetics & Genomic Medicine
|
November 26, 2024
Performance of Dysmorphology-Based Screening for Genetic Disorders in Pediatric Congenital Heart Disease Supports Wider Genetic Testing
Benjamin M Helm, Lindsey R Helvaty, Erin Conboy, et al.
Pediatric Research
|
January 7, 2026
Variant burden and severity of cardiomyopathy in patients with DMD-related Duchenne muscular dystrophy
Gabrielle C Geddes, Stephanie M Ware, Tae-Hwi Schwantes-An, et al.
Clinical Dysmorphology
|
September 14, 2020
Chromosome 4q28.3q32.3 duplication in a patient with lymphatic malformations, craniosynostosis, and dysmorphic features
Eric S Traub, Sarah E Sheppard, Yoav Dori, et al.
Heart Rhythm
|
September 28, 2014
Novel Timothy syndrome mutation leading to increase in CACNA1C window current
Nicole J Boczek, Erin M Miller, Dan Ye, et al.
Circulation. Genomic and Precision Medicine
|
August 20, 2021
Genetic Testing for Heritable Cardiovascular Diseases in Pediatric Patients: A Scientific Statement From the American Heart Association
Andrew P Landstrom, Jeffrey J Kim, Bruce D Gelb, et al.
Pediatric Research
|
February 8, 2025
Genomics of pediatric cardiomyopathy
Teresa M Lee, Stephanie M Ware, Alicia M Kamsheh, et al.
Journal of Cardiovascular Development and Disease
|
January 27, 2018
Rationale for the Cytogenomics of Cardiovascular Malformations Consortium: A Phenotype Intensive Registry Based Approach
Robert B Hinton, Kim L McBride, Steven B Bleyl, et al.
Development (Cambridge, England)
|
April 18, 2002
A complex syndrome of left-right axis, central nervous system and axial skeleton defects in Zic3 mutant mice
Smita M Purandare, Stephanie M Ware, Kin Ming Kwan, et al.
Circulation
|
October 26, 2005
Genetic predictors and remodeling of dilated cardiomyopathy in muscular dystrophy
John L Jefferies, Benjamin W Eidem, John W Belmont, et al.
Page
of 15
Search research articles
Search
Showing results (91-100 of 146) with videos related to
Sort By:
Page
of 15
The Journal of Clinical Investigation
|
July 30, 2024
Early ascertainment of genetic diagnoses clarifies impact on medium-term survival following neonatal congenital heart surgery
Benjamin J Landis, Benjamin M Helm, Matthew D Durbin, et al.
Molecular Genetics & Genomic Medicine
|
November 26, 2024
Performance of Dysmorphology-Based Screening for Genetic Disorders in Pediatric Congenital Heart Disease Supports Wider Genetic Testing
Benjamin M Helm, Lindsey R Helvaty, Erin Conboy, et al.
Pediatric Research
|
January 7, 2026
Variant burden and severity of cardiomyopathy in patients with DMD-related Duchenne muscular dystrophy
Gabrielle C Geddes, Stephanie M Ware, Tae-Hwi Schwantes-An, et al.
Clinical Dysmorphology
|
September 14, 2020
Chromosome 4q28.3q32.3 duplication in a patient with lymphatic malformations, craniosynostosis, and dysmorphic features
Eric S Traub, Sarah E Sheppard, Yoav Dori, et al.
Heart Rhythm
|
September 28, 2014
Novel Timothy syndrome mutation leading to increase in CACNA1C window current
Nicole J Boczek, Erin M Miller, Dan Ye, et al.
Circulation. Genomic and Precision Medicine
|
August 20, 2021
Genetic Testing for Heritable Cardiovascular Diseases in Pediatric Patients: A Scientific Statement From the American Heart Association
Andrew P Landstrom, Jeffrey J Kim, Bruce D Gelb, et al.
Pediatric Research
|
February 8, 2025
Genomics of pediatric cardiomyopathy
Teresa M Lee, Stephanie M Ware, Alicia M Kamsheh, et al.
Journal of Cardiovascular Development and Disease
|
January 27, 2018
Rationale for the Cytogenomics of Cardiovascular Malformations Consortium: A Phenotype Intensive Registry Based Approach
Robert B Hinton, Kim L McBride, Steven B Bleyl, et al.
Development (Cambridge, England)
|
April 18, 2002
A complex syndrome of left-right axis, central nervous system and axial skeleton defects in Zic3 mutant mice
Smita M Purandare, Stephanie M Ware, Kin Ming Kwan, et al.
Circulation
|
October 26, 2005
Genetic predictors and remodeling of dilated cardiomyopathy in muscular dystrophy
John L Jefferies, Benjamin W Eidem, John W Belmont, et al.
Page
of 15