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American Heart Journal|February 1, 1997
Hereditary bundle branch defect: right bundle branch blocks of different causes have different morphologic characteristicsE Stéphan, A de Meeus, P BouvagnetMammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1992
A detailed linkage map of subtelomeric murine chromosome 12 region including the situs inversus mutation locus IVA de Meeus, S Alonso, J Demaille, et al.Archives Des Maladies Du Coeur Et Des Vaisseaux|May 1, 1993
[Mice SI/Col: a study model in the research of genes involved in situs inversus]A de Meeus, S Alonso, J Demaille, et al.Archives Des Maladies Du Coeur Et Des Vaisseaux|May 1, 1996
[Genetics of hereditary cardiopathies]S Debrus, A de Meeus, M K Jean, et al.American Journal of Medical Genetics|February 11, 1997
Blastogenesis dominant 1: a sequence with midline anomalies and heterotaxyA de Meeus, P Sarda, R Tenconi, et al.Archives Des Maladies Du Coeur Et Des Vaisseaux|June 20, 2000
[Autosomal dominant Mendelian midline complex. Secundum atrial septal defect associated with cardiac and facial-thoracic defects. A familial case]E Stéphan, R Ashoush, A Mégarbané, et al.Circulation Research|October 1, 1995
An isolated cardiac conduction disease maps to chromosome 19qA de Meeus, E Stephan, S Debrus, et al.Herz|April 1, 1994
Deciphering the molecular genetics of congenital heart diseaseP Bouvagnet, U Sauer, S Debrus, et al.Human Genetics|February 1, 1996
Familial non-syndromic conotruncal defects are not associated with a 22q11 microdeletionS Debrus, G Berger, A de Meeus, et al.American Heart Journal|June 1, 1979
Hereditary bundle branch system defect. A new genetic entity?E StéphanPageof 6