Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
European Journal of Obstetrics, Gynecology, and Reproductive Biology|November 22, 2008
Impact of prenatal diagnosis of transposition of the great arteries on obstetric and early postnatal managementM J Raboisson, C Samson, C Ducreux, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|March 25, 2006
[Long QT syndrome in children: analysis of the Lyon series]M Iraqi, P Chevalier, M J Raboisson, et al.
Journal of Molecular Medicine (Berlin, Germany)|July 12, 2002
Expression and mutation analysis of BRUNOL3, a candidate gene for heart and thymus developmental defects associated with partial monosomy 10pP Lichtner, T Attié-Bitach, S Schuffenhauer, et al.
European Journal of Human Genetics : EJHG|September 12, 2000
X-linked transposition of the great arteries and incomplete penetrance among males with a nonsense mutation in ZIC3A Mégarbané, N Salem, E Stephan, et al.
Circulation Research|October 1, 1995
An isolated cardiac conduction disease maps to chromosome 19qA de Meeus, E Stephan, S Debrus, et al.
Circulation|December 10, 2003
Circumstances of death and gross and microscopic observations in a series of 200 cases of sudden death associated with arrhythmogenic right ventricular cardiomyopathy and/or dysplasiaA Tabib, R Loire, L Chalabreysse, et al.
American Journal of Human Genetics|March 7, 2001
Axonemal dynein intermediate-chain gene (DNAI1) mutations result in situs inversus and primary ciliary dyskinesia (Kartagener syndrome)C Guichard, M C Harricane, J J Lafitte, et al.
Herz|April 1, 1994
Deciphering the molecular genetics of congenital heart diseaseP Bouvagnet, U Sauer, S Debrus, et al.
Clinical Genetics|April 25, 2017
Truncating mutations on myofibrillar myopathies causing genes as prevalent molecular explanations on patients with dilated cardiomyopathyA Janin, K N'Guyen, G Habib, et al.
American Journal of Human Genetics|June 10, 2000
Mapping of a new locus for autosomal recessive demyelinating Charcot-Marie-Tooth disease to 19q13.1-13.3 in a large consanguineous Lebanese family: exclusion of MAG as a candidate geneV Delague, C Bareil, S Tuffery, et al.
Pageof 5