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Circulation|March 17, 1999
Homozygous deletion in KVLQT1 associated with Jervell and Lange-Nielsen syndromeQ Chen, D Zhang, R L Gingell, et al.
American Journal of Physiology. Heart and Circulatory Physiology|September 29, 2000
Novel characteristics of a misprocessed mutant HERG channel linked to hereditary long QT syndromeE Ficker, D Thomas, P C Viswanathan, et al.
Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi|February 18, 2004
Clinical profile and genetic basis of Brugada syndrome in the Chinese populationN S Mok, S G Priori, C Napolitano, 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.
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