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Circulation|August 1, 1985
Local changes in myosin types in diseased human atrial myocardium: a quantitative immunofluorescence studyP Bouvagnet, J Léger, C A Dechesne, et al.European Journal of Human Genetics : EJHG|February 15, 2001
Identification, tissue specific expression, and chromosomal localisation of several human dynein heavy chain genesA K Maiti, M G Mattéi, M Jorissen, 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.American Journal of Medical Genetics|March 30, 1999
Autosomal dominant secundum atrial septal defect with various cardiac and noncardiac defects: a new midline disorderA Mégarbané, E Stephan, R Kassab, et al.The European Respiratory Journal|March 7, 2008
Identification of transcripts overexpressed during airway epithelium differentiationB Chhin, J T Pham, L El Zein, et al.Journal of Dental Research|October 14, 2010
A new hypo/oligodontia syndrome: Carvajal/Naxos syndrome secondary to desmoplakin-dominant mutationsL Chalabreysse, F Senni, P Bruyère, et al.Archives Des Maladies Du Coeur Et Des Vaisseaux|June 20, 2000
[Cardiogenetics in the year 2000]S Pinson, C Guichard, D Lenoir, et al.Annals of Neurology|August 17, 2001
Nonprogressive autosomal recessive ataxia maps to chromosome 9q34-9qter in a large consanguineous Lebanese familyV Delague, C Bareil, P Bouvagnet, et al.Archives Des Maladies Du Coeur Et Des Vaisseaux|December 26, 2003
[Genetics and congenital heart diseases]F Sassolas, A Akhavi, C Mestrallet, et al.BMC Cardiovascular Disorders|March 8, 2023
Prenatal diagnosis of recurrent hypoplastic left heart syndrome associated with MYH6 variants: a case reportB Najib, T Quibel, A Tessier, et al.Pageof 5