Genetic heterogeneity and phenotypic anomalies in children with atrioventricular canal defect and tetralogy of Fallot-Reference-Cited by-同舟云学术

Genetic heterogeneity and phenotypic anomalies in children with atrioventricular canal defect and tetralogy of Fallot

Published:2006-04 Issue:2 Volume:15 Page:65-70
ISSN:0962-8827
Container-title:Clinical Dysmorphology
language:en
Short-container-title:

Author:

Vergara Pasquale,Digilio Maria Cristina,Zorzi Andrea De,Carlo Duccio Di,Capolino Rossella,Rimini Alessandro,Pelegrini Monica,Calabro` Raffaele,Marino Bruno

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics (clinical),General Medicine,Pathology and Forensic Medicine,Anatomy,Pediatrics, Perinatology and Child Health

Reference42 articles.

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2. 22q11 deletions in isolated and syndromic patients with tetralogy of Fallot;Amati;Hum Genet,1995

3. Pulmonary atresia with ventricular septal defect: prevalence of deletion 22q11 in the different anatomic pattern;Anaclerio;Ital Heart J,2001

4. Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways;Benson;J Clin Invest,1999

5. Surgical management of complete atrioventricular canal associated with tetralogy of Fallot;Bertolini;Cardiovasc Surg,1996

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