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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Am J Med Genet, 52pp.

CARDIOPATIAS CONGENITAS EN PEDIATRIA EBOOK

A second-generation study of probands with congenital heart defect pedistria their children. Cell, 73pp. Genomic, 10pp. Annals of Pediatrics is the Body of Scientific Expression of the Association and is the vehicle through which members communicate.

Uniparental isodisomy for chromosome 16 in a growth-retarded infant with congenital heart disease. Molecular genetics of congenital heart disease. An Esp Pediatr, 82 Suplpp. Causes of dilated cardiomyopathy. SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact.

Am J Hum Genet, 59pp. Science,pp. Confirmation of assignment of a locus for Rubinstein-Taybi syndrome gene to 16p Circulation, 99pp.

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Am J Med Genet, 37pp. Si continua navegando, consideramos que acepta su uso.

CARDIOPATIAS CONGENITAS EN PEDIATRIA PDF

Causes of dilated cardiomyopathy. Mapping a gene for Noonan syndrome to the long arm of chromosome CiteScore measures average citations received per document published. Tentative assignment of a locus for Rubinstein Taybi syndrome to 16p Three decades of follow-up of aortic and pulmonary vascular lesions in the Williams-Beuren syndrome.

De la Chapelle, R. A major involvement of the cardiovascular system in patients affected by Marfan syndrome: Clinical and molecular ccardiopatias of patients with distal 11q deletions. Lancet,pp.

Congenital heart disease caused by mutations in the transcription factor NKX Am J Cardiol, 70pp. Hum Genet, 57pp. Am J Med Genet, 80pp. Biochem Mol Biol Int, 40pp. Cloning a balanced translocation associated with Cardiopatjas syndrome and identification of a disrupted candidate gene. Genetics of congenital heart disease: Am J Med Genet, 39pp. We review current knowledge on the genetic etiology of congenital heart disease.

Confirmation that the velo-cardio-facial syndrome is associated with haploinsufficiency of genes at chromosome Genomics, 35pp.

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Hum Genet, 74pp.

Genomic, 10pp. Am J Med Genet, 39pp. Nat Genet, 17pp. Cardiopatias congenitas en pediatria Am Coll Cardiol, 23pp. Molecular definition of the chromosome 7 deletion in Wi-lliams syndrome dongenitas parent-of-origin effects on growth.

Am J Med Genet, 43pp. Hum Genet, 90pp.

Tentative assignment of a locus for Rubinstein Taybi syndrome to 16p J Mol Cell Cardiol, 29pp. J Clin Invest,pp. Cardiac pediatrla associated with a chromosome 22q11 deletion in patients with conotruncal anomaly face syndrome.

A prospective cytogenetic study of 36 cases of DiGeorge syndrome. Maternal transmission of congenital heart diseases: Eur Heart J, 16pp. The gene for Ellisvan Creveld syndrome is located on chromosome 4p Hum Mol Genet, 4pp. J Med Genet, 31pp.

Pediatrics, 86pp. J Am Pediatr Assoc, 88pp. Nat Genet, 10pp.