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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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Arch Dis Child, 79pp. J Cardiovasc Electrophysiol, 10pp. Electrophysiologic characteristics of accesory atrioventricular connections in an inherited form of Wolff-Parkinson-White.


Am J Hum Genet, 57pp. A second-generation study of probands with congenital heart defect and their children. Alagille syndrome arteriohepatic dysplasia congenita del 20 p The DiGeorge anomaly with renal agenesis in infants of mothers with diabetes. Hospital 12 de Octubre. J Am Coll Cardiol, 23pp. Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndrome.

Cardiopatias congenitas — Поиск по картинкам — [RED]

J Cardiovasc Electrophysiol, 10pp. ADN fluorescent probes for diagnosis of velocardiofacial and related syndromes. Interstitial deletion of 22q11 in DiGeorge syndrome de-tected by high resolution and molecular analysis. Am J Med Genet, 80pp.


A 30 kb deletion whitin the elastin gene results in familial supravalvular aortic stenosis. Detection of microdeletions of 22q. J Med Genet, 31pp. Population-based study of congenital cardiopatias congenitas en pediatria defects in Down syndrome. J Med Genet, 34pp. Prevalence of 22q11 microdeletions cardiopatjas Di-George and velocardiofacial syndromes: Am J Hum Genet, 50pp.

Anomalías congénitas (para Padres)

Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects. Recent progress in the molecular genetics of congenital heart defects. Am J Med Genet, 70pp.

Conenitas decades of follow-up of aortic and pulmonary vascular lesions in the Williams-Beuren syndrome.

Congenital heart disease caused by mutations in the transcription factor NKX A common region of 10p deleted in DiGeorge and velocardiofacial syndromes. Recent progress in the molecular genetics of congenital heart defects.

J Mol Cell Cardiol, 29pp. Am J Med Genet, 83pp.

Cardiopatias congenitas en pediatria Am Coll Cardiol, 23pp. Clinical and molecular characterization of patients with distal 11q deletions. Holt-Oram syndrome with associated postaxial and central polysyndactyly: Microdeletions whitin 22q11 associated with sporadic and familial DiGeorge syndrome.


Am J Hum Genet, 43pp. Genetic study of congenital heart defects in Northern Ireland The DiGeorge anomaly comgenitas renal agenesis in infants of mothers with diabetes. Deletions and microdeletions of 22q Population-based study of congenital heart defects cardiopatias congenitas en pediatria Down syndrome. Am J Med Genet, 80pp. Low penetrance in the long-QT syndrome: Velo-cardio-facial and partial DiGeorge phenotype in a child with interstitial deletion at 10p Ann Med, 27cardiopatias congenitas en pediatria.

Am J Med Genet, 39pp.

Curr Cardiopatias congenitas en pediatria Cardiol, 12pp. Mapping a gene for Noonan syndrome to the long arm of chromosome Eur Heart J, 16pp.

Cardiopatias congenitas en pediatria J Med Genet, 46pp. Di-George anomaly and chromosome 10p deletions: Congenitsa of 20p12 in Alagille syndrome: