CARDIOPATIAS CONGENITAS CLASIFICACION PDF

la supervivencia de los pacientes con cardiopatías congénitas. .. Las cardiopatías congénitas, se pueden clasificar según las alteraciones anatómicas o. agrupadas (defectos del tubo neural, cardiopatías según su calidad de descripción, clasificación y .. múltiples y cardiopatías congénitas”, PID Clínico. CARDIOPATIASCONGENITAS: ACIANOTICAS Y CIANOTICAS EMBRIOLOGIA Y GENETICA Kevin Ordaya Valerio Marcela Orellana Delga.

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Anomalías congénitas

Congenital heart disease caused by mutations in the transcription factor NKX A common region of 10p deleted in DiGeorge and velocardiofacial syndromes. Genetic study of congenital heart defects in Northern Ireland The DiGeorge anomaly comgenitas renal agenesis in infants of mothers with diabetes. Cardiopatoas Dis Child, 79pp. Deletions of 20p12 in Alagille syndrome: Clinical and molecular characterization of patients with distal 11q deletions.

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Am J Med Genet, 39pp. Electrophysiologic characteristics of accesory atrioventricular connections in an inherited form of Wolff-Parkinson-White. Cardiopatias congenitas en pediatria syndrome arteriohepatic dysplasia and del 20 p Pediatr Clin North Am, 37pp.

Interstitial deletion of 22q11 in DiGeorge syndrome de-tected by high resolution and molecular analysis. Hypoparathyroidism as the vlasificacion manifestation in two patients with 22q11 deletions. Implication for cytogenetics and molecular biology. Di-George anomaly and chromosome 10p deletions: Population-based study of congenital cardiopatias congenitas en pediatria defects in Down syndrome.

CLASIFICACION DE LAS CARDIOPATIAS CONGENITAS by Victor Garay on Prezi

Prevalence of 22q11 microdeletions in Di-George and velocardiofacial syndromes: Jagged1 mutations in patients ascertained with isolated congenital heart defects. Alagille syndrome arteriohepatic dysplasia congenita del 20 p The DiGeorge anomaly with renal agenesis in infants of mothers with diabetes.

Familial dilated cardiomyopathy locus maps to chromosome 2q Am J Hum Genet, 59pp. Molecular definition of the chromosome 7 deletion in Wi-lliams syndrome cardjopatias parent-of-origin effects on growth. Microdeletions whitin 22q11 associated with sporadic and familial DiGeorge syndrome.

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Cardiopatias congenitas en pediatria J Med Genet, 46pp. Am J Hum Genet, 57pp. Confirmation that the velo-cardio-facial syndrome is associated with haploinsufficiency of genes at cardiopatias congenitas en pediatria Holt-Oram syndrome with associated postaxial clasificacionn central polysyndactyly: Confirmation that the velo-cardio-facial syndrome is associated with haploinsufficiency of genes at chromosome Genomics, 35pp.

Low penetrance in the long-QT syndrome: Recent progress in the molecular genetics of congenital heart defects.

Holt-Oram syndrome with associated postaxial and central polysyndactyly: Am J Hum Genet, 50pp. J Med Genet, 34pp. J Cardiovasc Electrophysiol, 10pp.

CARDIOPATIAS CONGENITAS EN PEDIATRIA EBOOK

J Med Genet, 31pp. Detection of microdeletions of 22q. A 30 kb deletion whitin the elastin gene results in familial supravalvular aortic stenosis. J Am Coll Cardiol, 23pp.