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Evaluación Radiológica de las Cardiopatias Congenitas. 1. Cardiopatías Congénitas; 2. Cardiopatías Congénitas Incidencia 8 de cada. Primer sitio Web en Argentina sobre cardiopatías congénitas.

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Eur J Pediatr,pp. Science,pediatira. GATA4 haploinsufficiency in patients with interstitial deletion of chromosome region 8p Hospital 12 de Octubre.

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Fibrillin-1 mutations in Marfan syn-drome and other type-1 fibrillinopathies. Electrophysiologic characteristics of accesory atrioventricular connections in an inherited form of Wolff-Parkinson-White. SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact. Patterns of autosomal dominant, autosomal recessive pwdiatria X-linked inheritance have been described. Subscribe to our Newsletter.

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To improve our services and products, we use “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior. Pediatr Clin North Am, 37pp.


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A submicroscopic deletion in Xq26 associated with familial situs ambiguous. Holt-Oram syndrome with associated postaxial and pediatris polysyndactyly: Interstitial deletion of 22q11 in DiGeorge syndrome de-tected by high resolution and molecular analysis. Familial dilated cardiomyopathy locus maps to chromosome 2q The elastin gene is disrupted by a translocation associated ;ediatria supravalvular aortic stenosis. Clinical and molecular characterization of patients with distal 11q deletions. Am J Med Genet, 73pp.

Nat Genet, 8pp. Am J Med Genet, 80pp. Jagged1 mutations in patients ascertained with isolated congenital heart defects. Three decades of follow-up of aortic and pulmonary vascular lesions in the Williams-Beuren syndrome. Evidence of genetic heterogeneity in RomanoWard long QT syndrome: