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Circulation|September 7, 2000
Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2I Splawski, J Shen, K W Timothy, et al.
Circulation|March 17, 1999
Homozygous deletion in KVLQT1 associated with Jervell and Lange-Nielsen syndromeQ Chen, D Zhang, R L Gingell, et al.
Journal of the American College of Cardiology|January 1, 1997
Age-gender influence on the rate-corrected QT interval and the QT-heart rate relation in families with genotypically characterized long QT syndromeM H Lehmann, K W Timothy, D Frankovich, et al.
The New England Journal of Medicine|October 1, 1998
Influence of the genotype on the clinical course of the long-QT syndrome. International Long-QT Syndrome Registry Research GroupW Zareba, A J Moss, P J Schwartz, et al.
Circulation|August 2, 2001
Clinical implications for affected parents and siblings of probands with long-QT syndromeJ Kimbrough, A J Moss, W Zareba, et al.
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