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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.
European Heart Journal|December 1, 1984
Characterization and distribution of myosin variants in normal and pathological human heartsJ Léger, C Dechesne, P Bouvagnet, et al.
Circulation Research|December 1, 1984
Fiber types and myosin types in human atrial and ventricular myocardium. An anatomical descriptionP Bouvagnet, J Leger, F Pons, et al.
European Journal of Clinical Investigation|December 1, 1985
Levels of ventricular myosin fragments in human sera after myocardial infarction, determined with monoclonal antibodies to myosin heavy chainsJ O Leger, P Bouvagnet, B Pau, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 16, 2018
Recurrent F8 and F9 gene variants result from a founder effect in two large French haemophilia cohortsF Lassalle, O Marmontel, C Zawadzki, et al.
Basic Research in Cardiology|January 1, 1989
Distribution pattern of alpha and beta myosin in normal and diseased human ventricular myocardiumP Bouvagnet, H Mairhofer, J O Leger, et al.
European Journal of Medical Genetics|February 9, 2012
Molecular characterization of a large MYBPC3 rearrangement in a cohort of 100 unrelated patients with hypertrophic cardiomyopathyV Chanavat, M F Seronde, P Bouvagnet, et al.
American Journal of Medical Genetics|February 11, 1997
Autosomal recessive lateralization and midline defects: blastogenesis recessive 1S Debrus, U Sauer, S Gilgenkrantz, et al.
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