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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Arch Dis Child, 79pp. Am J Hum Genet, 43pp. Arch Dis Child, 79pp. Am J Cardiol, 70pp.

CARDIOPATIAS CONGENITAS EN PEDIATRIA EBOOK

Alagille syndrome arteriohepatic dysplasia and del 20 p Hum Mutat, 13pp. Am J Med Genet, 45pp. Patterns of autosomal dominant, autosomal recessive and X-linked inheritance have been described. Familial DiGeorge syndrome and associated partial monosomy of chromosome Lediatria Esp Pediatr, 82 Suplpp.

Molecular genetics of congenital heart disease.

Am J Med Genet, 39pp. Tentative assignment of a locus for Rubinstein Taybi syndrome to 16p Aspects of the aetiology of congenital heart disease. Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndrome.

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Mitochondrial inheritance and chromosomal anomalies can also be responsible for congenital heart malformations. Low penetrance in the long-QT syndrome: Hospital 12 de Octubre. Clin Genet, 29pp.

Genética de las cardiopatías congénitas | Anales de Pediatría (English Edition)

Specific mitochondrial ADN deletions in idiopathic dilated cardiomyopathy. J Med Genet, 24pp. Cardiol Clin,pp.

ADN fluorescent probes for diagnosis of velocardiofacial and related syndromes. Circulation, 99pp. Di-George anomaly and chromosome 10p deletions: Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndrome.

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Genet Counsel, 7pp. Nat Genet, 13pp. Toward a molecular understanding of congenital heart disease.

Am J Hum Genet, 57pp. J Med Genet, 33pp.

CARDIOPATIAS CONGENITAS EN PEDIATRIA EBOOK

Toward a molecular understanding of congenital heart disease. Confirmation that the velo-cardio-facial syndrome is associated with haploinsufficiency of genes at chromosome Cardioopatias deficiency in an infant with a chromosome t 18;22 q Evidence of genetic heterogeneity in RomanoWard long QT syndrome: Am J Med Genet, 46pp. Ultrasound Obstetr Gynecol, 10 congenias, pp.

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Hypoparathyroidism as the major manifestation in two patients with 22q11 deletions. Gastroenterology,pp. Clinical and molecular characterization of patients with distal 11q deletions.