22q11 deletions in isolated and syndromic patients with tetralogy of Fallot-Reference-Cited by-同舟云学术

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22q11 deletions in isolated and syndromic patients with tetralogy of Fallot

Published:1995-05 Issue:5 Volume:95 Page:
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Amati Francesca,Mari Aldo,Digilio MariaCristina,Mingarelli Rita,Marino Bruno,Giannotti Aldo,Novelli Giuseppe,Dallapiccola Bruno

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00223856.pdf

Cited by 86 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. Multiple Major Aortopulmonary Collateral Arteries With Tetralogy of Fallot and Other Congenital Cardiac Disorders Detected in the Fourth Decade: A Report of a Rare Case;Cureus;2024-06-26

2. Comparison of Postoperative, In-Hospital Outcomes After Complete Repair of Tetralogy of Fallot Between 22q11.2 Deletion Syndrome and Trisomy 21;Pediatric Cardiology;2021-07-30

3. Ontogeny of the facial phenotypic variability in Mexican patients with 22q11.2 deletion syndrome;Head & Face Medicine;2019-12

4. A Comparative Study of Histopathological Changes in the Ascending Aorta and the Risk Factors Related to Histopathological Conditions and Aortic Dilatation in Patients With Tetralogy of Fallot and a Functionally Univentricular Heart;Heart, Lung and Circulation;2018-08

5. Heterozygous missense mutations in NFATC1 are associated with atrioventricular septal defect;Human Mutation;2018-07-30

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