Review
doi: 10.1136/hrt.2009.190090.
Use and interpretation of genetic tests in cardiovascular genetics
Affiliations
- PMID: 20937756
- DOI: 10.1136/hrt.2009.190090
Item in Clipboard
Review
Use and interpretation of genetic tests in cardiovascular genetics
Heart.
2010 Oct.
No abstract available
Similar articles
-
[Hereditary risk of sudden cardiac death--genetic investigation of the family].Lakartidningen. 2009 Apr 7-21;106(15-16):1089-93. Lakartidningen. 2009. PMID: 19492675 Review. Swedish. No abstract available.
-
Molecular genetics of arrhythmias and cardiovascular conditions associated with arrhythmias.J Cardiovasc Electrophysiol. 2003 Nov;14(11):1259-72. doi: 10.1046/j.1540-8167.2003.03316.x. J Cardiovasc Electrophysiol. 2003. PMID: 14678150 Review. No abstract available.
-
Recent progress in the genetics of cardiomyopathy and its role in the clinical evaluation of patients with cardiomyopathy.Curr Opin Cardiol. 2011 Mar;26(2):155-64. doi: 10.1097/HCO.0b013e3283439797. Curr Opin Cardiol. 2011. PMID: 21297463 Review.
-
Guidelines for the diagnosis and management of familial dilated cardiomyopathy.Heart Lung Circ. 2007 Feb;16(1):19-21. doi: 10.1016/j.hlc.2006.10.018. Epub 2006 Dec 26. Heart Lung Circ. 2007. PMID: 17188933 No abstract available.
-
Plan of Action for Inherited Cardiovascular Diseases: Synthesis of Recommendations and Action Algorithms.Rev Esp Cardiol (Engl Ed). 2016 Mar;69(3):300-9. doi: 10.1016/j.rec.2015.11.029. Epub 2016 Feb 6. Rev Esp Cardiol (Engl Ed). 2016. PMID: 26856793
Cited by
-
A clinical approach to inherited hypertrophy: the use of family history in diagnosis, risk assessment, and management.Circ Cardiovasc Genet. 2013 Feb;6(1):118-31. doi: 10.1161/CIRCGENETICS.110.959387. Circ Cardiovasc Genet. 2013. PMID: 23424256 Free PMC article. Review. No abstract available.
-
Factors Associated with Uptake of Genetics Services for Hypertrophic Cardiomyopathy.J Genet Couns. 2015 Oct;24(5):797-809. doi: 10.1007/s10897-014-9810-8. Epub 2015 Jan 8. J Genet Couns. 2015. PMID: 25566741
-
Consensus: a framework for evaluation of uncertain gene variants in laboratory test reporting.Genome Med. 2012 May 28;4(5):48. doi: 10.1186/gm347. Genome Med. 2012. PMID: 22640420 Free PMC article.
-
Usability of a novel clinician interface for genetic results.J Biomed Inform. 2012 Oct;45(5):950-7. doi: 10.1016/j.jbi.2012.03.007. Epub 2012 Apr 12. J Biomed Inform. 2012. PMID: 22521718 Free PMC article.
-
Re-examining the Ethics of Genetic Counselling in the Genomic Era.J Bioeth Inq. 2020 Sep;17(3):325-335. doi: 10.1007/s11673-020-09983-w. Epub 2020 Jun 15. J Bioeth Inq. 2020. PMID: 32557217 Free PMC article.
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
