Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference24 articles.
1. Neubauer J, Haas C, Bartsch C, Medeiros-Domingo A, Berger W. Post-mortem whole-exome sequencing (WES) with a focus on cardiac disease-associated genes in five young sudden unexplained death (SUD) cases. Int J Legal Med. 2016;130:1011–21.
2. Ouellette AC, Mathew J, Manickaraj AK, Manase G, Zahavich L, Wilson J, et al. Clinical genetic testing in pediatric cardiomyopathy: is bigger better? Clin Genet. 2018;93:33–40.
3. Cirino AL, Lakdawala NK, McDonough B, Conner L, Adler D, Weinfeld M, et al. A comparison of whole genome sequencing to multigene panel testing in hypertrophic cardiomyopathy patients. Circul Cardiovasc Genet. 2017;10:e001768.
4. Gómez J, Reguero JR, Coto E. The ups and downs of genetic diagnosis of hypertrophic cardiomyopathy. Rev Esp Cardiol. 2016;69:61–8.
5. Michels M, Soliman OI, Phefferkorn J, Hoedemaekers YM, Kofflard MJ, Dooijes D, et al. Disease penetrance and risk stratification for sudden cardiac death in asymptomatic hypertrophic cardiomyopathy mutation carriers. Eur Heart J. 2009;30:2593–8.
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