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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 genomes
G 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 1
C 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 Xq28
J 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 disease
H 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 pattern
S Evain, F Briec, F Kyndt, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 25) with videos related to
Sort By:
Page
of 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 genomes
G 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 1
C 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 Xq28
J 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 disease
H 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 pattern
S Evain, F Briec, F Kyndt, et al.
Page
of 3