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Journal of Cardiovascular Development and Disease|January 26, 2018
Dystrophic Cardiomyopathy: Complex Pathobiological Processes to Generate Clinical PhenotypeTakeshi Tsuda, Kristi K FitzgeraldReviews in Cardiovascular Medicine|July 25, 2020
Sudden cardiac death in children and young adults without structural heart disease: a comprehensive reviewTakeshi Tsuda, Kristi K Fitzgerald, Joel TemplePediatric Cardiology|January 19, 2024
Diverse Cardiac Phenotype of Becker Muscular Dystrophy: Under-Recognized Subclinical Cardiomyopathy Due to Partial Dystrophin Deficiency in a Contemporary EraPriya Nigam, Kristi K Fitzgerald, Mena Scavina, et al.Case Reports in Genetics|April 9, 2014
Novel SMAD3 Mutation in a Patient with Hypoplastic Left Heart Syndrome with Significant Aortic AneurysmKristi K Fitzgerald, Abdul Majeed Bhat, Katrina Conard, et al.American Journal of Medical Genetics. Part A|October 24, 2020
Inherited intragenic PBX1 deletion: Expanding the phenotypeKristi K Fitzgerald, Nina Powell-Hamilton, Amanda J Shillingford, et al.JCI Insight|July 15, 2020
Molecular characterization of the calcium release channel deficiency syndromeDavid J Tester, C S John Kim, Samantha K Hamrick, et al.Journal of Genetic Counseling|September 12, 2021
Genetic counseling for congenital heart disease - Practice resource of the National Society of Genetic CounselorsHannah E Ison, Emily L Griffin, Ashley Parrott, et al.JAMA Cardiology|January 9, 2020
Identification of a Novel Homozygous Multi-Exon Duplication in RYR2 Among Children With Exertion-Related Unexplained Sudden Deaths in the Amish CommunityDavid J Tester, Hannah M Bombei, Kristi K Fitzgerald, et al.American Journal of Human Genetics|June 21, 2008
Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11Christian R Marshall, Edwin J Young, Ariel M Pani, et al.American Journal of Human Genetics|January 11, 2025
DNA-binding affinity and specificity determine the phenotypic diversity in BCL11B-related disordersIvana Lessel, Anja Baresic, Ivan K Chinn, et al.Pageof 1