Showing results (1-10 of 34) with videos related to
Sort By:
Pageof 4
European Heart Journal. Case Reports|December 3, 2021
A case report of <i>RASA1</i>-associated inherited lymphoedema with recurrent life-threatening lymphangitisDominik S Westphal, Katharina Bergmann, Eimo Martens, et al.Frontiers in Genetics|April 11, 2018
<i>MAP2</i> - A Candidate Gene for Epilepsy, Developmental Delay and Behavioral Abnormalities in a Patient With Microdeletion 2q34Dominik S Westphal, Stephanie Andres, Christine Makowski, et al.Case Reports in Cardiology|March 27, 2023
The Role of <i>RYR2</i> in Atrial FibrillationBernhard M Boehm, Jochen Gaa, Petra Hoppmann, et al.Gene|March 25, 2017
Identification of a de novo microdeletion 1q44 in a patient with hypogenesis of the corpus callosum, seizures and microcephaly - A case reportDominik S Westphal, Stephanie Andres, Kirsten I Beitzel, et al.Molecular Genetics & Genomic Medicine|May 9, 2020
Reclassification of genetic variants in children with long QT syndromeDominik S Westphal, Tobias Burkard, Alexander Moscu-Gregor, et al.Gene|January 7, 2022
There is more to it than just congenital heart defects - The phenotypic spectrum of TAB2-related syndromeDominik S Westphal, Elisa Mastantuono, Heide Seidel, et al.Gene|April 5, 2022
Myocarditis or inherited disease? - The multifaceted presentation of arrhythmogenic cardiomyopathyDominik S Westphal, Hannah Krafft, Ruth Biller, et al.Gene|November 1, 2024
Variants that get straight to your heart - Cardiogenetic secondary findings in exome sequencingKirsten Wenderholm, Theresa Brunet, Elisabeth Graf, et al.Cardiology in the Young|September 27, 2021
Do children with congenital heart defects meet the vaccination recommendations? Immunisation in children with congenital heart defectsJulia Remmele, Dominik S Westphal, Carolin Unterleitner, et al.Journal of Clinical Medicine|December 11, 2022
Fetal Bradycardia Caused by Monogenic Disorders-A Review of the LiteratureDominik S Westphal, Michael Hauser, Britt-Maria Beckmann, et al.Pageof 4