CARDIOPATIAS CONGENITAS EN PEDIATRIA PDF

CARDIOPATIAS CONGENITAS EN PEDIATRIA PDF

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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Hum Genet, 57pp.

Cardiopatías Congénitas · CardioCongénitas

An Esp Pediatr, 44pp. ADN fluorescent probes for diagnosis of velocardiofacial and related syndromes. J Cardiopatisa Cell Cardiol, 29pp. Am J Med Genet, 29pp. J Am Coll Cardiol, 23pp.

CARDIOPATIAS CONGENITAS EN PEDIATRIA EBOOK

An Esp Pediatr, 82 Suplpp. Cell, 73pp. J Clin Invest,pp.

Molecular definition of the chromosome 7 deletion in Wi-lliams syndrome and parent-of-origin effects on growth. Am J Hum Genet, 61pp. Biochem Mol Biol Int, 40pp.

Clin Genet, 46pp. Genes Dev, 12pp. Hypoparathyroidism as the major manifestation in two patients with 22q11 deletions.

A genetic etiology for DiGeorge syndrome: Low penetrance in the long-QT syndrome: A submicroscopic deletion in Xq26 associated with familial situs ambiguous. Three decades of follow-up of aortic and pulmonary vascular lesions in the Williams-Beuren syndrome.

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caardiopatias Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q Detection of microdeletions of 22q You can change the settings or obtain more information by clicking here.

Alagille syndrome arteriohepatic dysplasia and del 20 p A second-generation study of probands with congenital heart defect and their children. Hospital 12 de Octubre. Am J Hum Genet, 43pp.

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Hum Genet, 96pp. Am J Cardiol, 59pp.

Recent progress in the molecular genetics of congenital heart defects. Mapping a gene for Noonan syndrome to the long arm of chromosome Microdeletions of chromosome 22 in patients with conotruncal cardiac defects.

Mapping a gene for Noonan syndrome to the long arm of chromosome The compulsion of chirality: A common region of 10p deleted in DiGeorge and velocardiofacial syndromes. Hum Mol Genet, 4pp.