Identificación de genes candidatos en las comunicaciones interventriculares congénitas con pérdida de heterocigosis de HSA22q11
Author:
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine
Reference39 articles.
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3. Monosomy 22q11 in patients with pulmonary atresia, ventricular septal defect, and major aortopulmonary collateral arteries;Hofbeck;Heart,1998
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1. Genetic testing for ventricular septal defect;The EuroBiotech Journal;2018-09-01
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3. Avances en genética molecular de las cardiopatías congénitas;Revista Española de Cardiología;2009-03
4. Advances in Molecular Genetics of Congenital Heart Disease;Revista Española de Cardiología (English Edition);2009-03
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