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Archives Des Maladies Du Coeur Et Des Vaisseaux
|
May 1, 1991
[Idiopathic dilated cardiomyopathies in children. Development and prognostic factors]
S Di Filippo, A Bozio, J Normand, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux
|
February 1, 1995
[Thrombolytic therapy with rt-PA for thrombosis of tricuspid valve prosthesis during pregnancy]
O Azzano, P French, J Robin, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux
|
February 1, 1985
[Congenital aortic valve stenosis. Long-term results after valvulotomy]
G Champsaur, J Ninet, J P Frieh, et al.
Human Genetics
|
February 1, 1996
Familial non-syndromic conotruncal defects are not associated with a 22q11 microdeletion
S Debrus, G Berger, A de Meeus, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux
|
June 25, 2004
[Neonatal forms of congenital long QT syndrome]
J M Lupoglazoff, I Denjoy, E Villain, et al.
Journal of Molecular and Cellular Cardiology
|
May 1, 1997
Lack of evidence for connexin 43 gene mutations in human autosomal recessive lateralization defects
S Debrus, S Tuffery, R Matsuoka, et al.
Page
of 10
Search research articles
Search
Showing results (91-100 of 96) with videos related to
Sort By:
Page
of 10
You have reached the last page of results.
This site can display upto 96 results.
Archives Des Maladies Du Coeur Et Des Vaisseaux
|
May 1, 1991
[Idiopathic dilated cardiomyopathies in children. Development and prognostic factors]
S Di Filippo, A Bozio, J Normand, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux
|
February 1, 1995
[Thrombolytic therapy with rt-PA for thrombosis of tricuspid valve prosthesis during pregnancy]
O Azzano, P French, J Robin, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux
|
February 1, 1985
[Congenital aortic valve stenosis. Long-term results after valvulotomy]
G Champsaur, J Ninet, J P Frieh, et al.
Human Genetics
|
February 1, 1996
Familial non-syndromic conotruncal defects are not associated with a 22q11 microdeletion
S Debrus, G Berger, A de Meeus, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux
|
June 25, 2004
[Neonatal forms of congenital long QT syndrome]
J M Lupoglazoff, I Denjoy, E Villain, et al.
Journal of Molecular and Cellular Cardiology
|
May 1, 1997
Lack of evidence for connexin 43 gene mutations in human autosomal recessive lateralization defects
S Debrus, S Tuffery, R Matsuoka, et al.
Page
of 10