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Methods
Short report
Rapid detection of genetic variants in hypertrophic cardiomyopathy by custom DNA resequencing array in clinical practice
- Correspondence to Dr Siv Fokstuen, Genetic Medicine, Centre Médical Universitaire, 1 rue Michel-Servet, 1211 Geneva 4, Switzerland; siv.fokstuen{at}unige.ch
Citation
Rapid detection of genetic variants in hypertrophic cardiomyopathy by custom DNA resequencing array in clinical practice
Publication history
- Received July 22, 2010
- Accepted November 18, 2010
- First published January 14, 2011.
Online issue publication
July 21, 2011
Article Versions
- Previous version (14 January 2011).
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© 2011, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.