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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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Arch Dis Child, 63pp.

CARDIOPATIAS CONGENITAS EN PEDIATRIA EBOOK

Am J Hum Genet, 57pp. Results of chromosomal analysis in fetuses with cardiac anomalies as diagnosed by first and early second-trimester echocar-diography.

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

J Med Genet, 34pp. Genomics, 35pp. Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q Lancet,pp. A second-generation study of probands with congenital heart defect and peediatria children. Mitochondrial inheritance and chromosomal anomalies can also be responsible for congenital heart malformations.

Circulation, peduatriapp. The gene for Ellisvan Creveld syndrome is located on chromosome 4p Curr Op Cardiol, 12pp. Diagnosis and management of infantile Marfan syndrome.

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CARDIOPATIAS CONGENITAS EN PEDIATRIA EBOOK

Am J Med Genet, 65pp. Am J Hum Genet, 61pp. Mapping of microsatellite markers in the Alagille region and screening of microdeletions by genotyping 23 patients. Confirmation of assignment of a locus for Rubinstein-Taybi syndrome gene to 16p Di-George anomaly and chromosome 10p deletions: A second-generation study of probands with congenital heart defect and their children.

Deletions of 20p12 in Alagille syndrome: J Clin Invest,pp. Eur J Hum Genet, 2pp.

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.

Ann Med, 27pp. J Med genet, 31pp.

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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Recurrence risk in offspring of adults with major heart defects: Hum Genet, 57pp. Ann Med, 27pp. Ultrasound Obstetr Gynecol, 10pp.

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: