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J J Schott

Showing results (1-10 of 25) with videos related to

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Archives Des Maladies Du Coeur Et Des Vaisseaux|April 1, 1997
[Hereditary cardiac arrhythmia]H Le Marec, J J Schott
Archives Des Maladies Du Coeur Et Des Vaisseaux|June 1, 1997
[Congenital long QT syndromes]H Le Marec, J J Schott
Journal Des Maladies Vasculaires|April 13, 2006
[Heredity and genetic aspects of Raynaud's disease]M A Pistorius, B Planchon, J J Schott, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|December 26, 2003
[Genetic aspects of cardiac conduction defects]V Probst, F Kyndt, M Allouis, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|December 26, 2003
[Genetics and cardiac arrhythmias]V Probst, F Kyndt, M Allouis, et al.
EXS|January 1, 1993
Detection, cloning, and distribution of minisatellites in some mammalian genomesG Vergnaud, D Gauguier, J J Schott, et al.
American Journal of Human Genetics|May 22, 2002
Familial deafness, congenital heart defects, and posterior embryotoxon caused by cysteine substitution in the first epidermal-growth-factor-like domain of jagged 1C Le Caignec, M Lefevre, J J Schott, et al.
Journal of the American College of Cardiology|June 7, 2000
Clinical characteristics of a familial inherited myxomatous valvular dystrophy mapped to Xq28J N Trochu, F Kyndt, J J Schott, et al.
The Journal of Clinical Investigation|July 21, 2000
Loss of function and inhibitory effects of human CSX/NKX2.5 homeoprotein mutations associated with congenital heart diseaseH Kasahara, B Lee, J J Schott, et al.
Heart Rhythm|November 6, 2008
Sodium channel blocker tests allow a clear distinction of electrophysiological characteristics and prognosis in patients with a type 2 or 3 Brugada electrocardiogram patternS Evain, F Briec, F Kyndt, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Archives Des Maladies Du Coeur Et Des Vaisseaux|April 1, 1997
[Hereditary cardiac arrhythmia]H Le Marec, J J Schott
Archives Des Maladies Du Coeur Et Des Vaisseaux|June 1, 1997
[Congenital long QT syndromes]H Le Marec, J J Schott
Journal Des Maladies Vasculaires|April 13, 2006
[Heredity and genetic aspects of Raynaud's disease]M A Pistorius, B Planchon, J J Schott, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|December 26, 2003
[Genetic aspects of cardiac conduction defects]V Probst, F Kyndt, M Allouis, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|December 26, 2003
[Genetics and cardiac arrhythmias]V Probst, F Kyndt, M Allouis, et al.
EXS|January 1, 1993
Detection, cloning, and distribution of minisatellites in some mammalian genomesG Vergnaud, D Gauguier, J J Schott, et al.
American Journal of Human Genetics|May 22, 2002
Familial deafness, congenital heart defects, and posterior embryotoxon caused by cysteine substitution in the first epidermal-growth-factor-like domain of jagged 1C Le Caignec, M Lefevre, J J Schott, et al.
Journal of the American College of Cardiology|June 7, 2000
Clinical characteristics of a familial inherited myxomatous valvular dystrophy mapped to Xq28J N Trochu, F Kyndt, J J Schott, et al.
The Journal of Clinical Investigation|July 21, 2000
Loss of function and inhibitory effects of human CSX/NKX2.5 homeoprotein mutations associated with congenital heart diseaseH Kasahara, B Lee, J J Schott, et al.
Heart Rhythm|November 6, 2008
Sodium channel blocker tests allow a clear distinction of electrophysiological characteristics and prognosis in patients with a type 2 or 3 Brugada electrocardiogram patternS Evain, F Briec, F Kyndt, et al.
Pageof 3