Genetic testing for atrioventricular septal defect
Author:
Affiliation:
1. MAGI’s Lab , Rovereto , Italy
2. MAGI Euregio , Bolzano , Italy
3. Department of Pharmaceutical Sciences , University of Perugia , Perugia , Italy
4. Department of Medical Genetics , Erciyes University Medical School , Kayseri , Turkey
Abstract
Publisher
Walter de Gruyter GmbH
Subject
Genetics,Molecular Biology,Biomedical Engineering,Molecular Medicine,Food Science,Biotechnology
Link
https://www.sciendo.com/pdf/10.2478/ebtj-2018-0036
Reference11 articles.
1. Craig B. Atrioventricular septal defect: from fetus to adult. Heart 2006; 92(12): 1879-85.1710589710.1136/hrt.2006.093344
2. Ferencz C, Boughman JA, Neill CA, Brenner JI, Perry LW. Congenital cardiovascular malformations: questions on inheritance. Baltimore-Washington Infant Study Group. J Am Coll Cardiol 1989; 14(3): 756-63.10.1016/0735-1097(89)90122-8
3. Feldt RH, O’Connell EJ, Stickler GB, Weidman WH. Etiologic factors in congenital heart disease. Am J Dis Child 1968; 115(5): 552-556.10.1001/archpedi.1968.021000105540045689488
4. Disegni E, Pierpont ME, Bass JL, Kaplinsky E. Two-dimensional echocardiography in detection of endocardial cushion defect in families. Am J Cardiol 1985; 55(13 Pt 1): 1649-52.10.1016/0002-9149(85)90998-14003317
5. Digilio MC, Marino B, Cicini MP, Giannotti A, Formigari R, et al. Risk of congenital heart defects in relatives of patients with atrioventricular canal. Am J Dis Child 1993; 147(12): 1295-97.8249947
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