Deficiency of the infundibular septum in patients with Interrupted aortic arch and del 22q11-Reference-Cited by-同舟云学术

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Deficiency of the infundibular septum in patients with Interrupted aortic arch and del 22q11

Published:2000-07 Issue:4 Volume:10 Page:428-429
ISSN:1047-9511
Container-title:Cardiology in the Young
language:en
Short-container-title:Cardiol Young

Author:

Marino B.,Digilio M.C.,Toscano A.,Dallapiccola B.

Publisher

Cambridge University Press (CUP)

Subject

Cardiology and Cardiovascular Medicine,General Medicine,Pediatrics, Perinatology and Child Health

Reference14 articles.

1. Association of interrupted aortic arch with malformations producing reduced blood flow to the fourth aortic arches

2. Comparison of occurrence of genetic syndromes in ventricular septal defect with pulmonic stenosis (classic tetralogy of Fallot) versus ventricular septal defect with pulmonic atresia

3. Truncus Arteriosus Communis Associated With Chromosome 22q11 Deletion

4. Associated cardiac anomalies in isolated and syndromic patients with tetralogy of fallot

5. Ventricular septal defect in interruption of aortic arch

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. 22q11.2 Deletion Syndrome: Impact of Genetics in the Treatment of Conotruncal Heart Defects;Children;2022-05-25

2. Clinical Manifestations of 22q11.2 Deletion Syndrome;Heart Failure Clinics;2022-01

3. Congenital heart disease and cardiovascular abnormalities associated with 22q11.2 deletion syndrome;The Chromosome 22q11.2 Deletion Syndrome;2022

4. Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers;American Journal of Medical Genetics Part A;2018-04-16

5. Congenital heart disease and genetic syndromes: new insights into molecular mechanisms;Expert Review of Molecular Diagnostics;2017-08-03

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