Fetal aortic root dilation: a prenatal feature of the Loeys-Dietz syndrome-Reference-Cited by-同舟云学术

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Fetal aortic root dilation: a prenatal feature of the Loeys-Dietz syndrome

Published:2006 Issue:11 Volume:26 Page:1081-1083
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Viassolo Valeria,Lituania Mario,Marasini Maurizio,Dietz Harry,Benelli Fabrizio,Forzano Francesca,Faravelli Francesca

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Reference6 articles.

1. Isolated ductus arteriosus aneurysm in the fetus and infant: a multi-institutional experience

2. Diagnosis of fetal ductus arteriosus aneurysm: importance of the three-vessel view

3. A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2

4. Echocardiographic diagnosis of fetal marfan syndrome at 34 weeks' gestation

5. Heterozygous TGFBR2 mutations in Marfan syndrome

Cited by 35 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. Cleft Palate and Aortic Dilatation as Clues for Loeys–Dietz Syndrome;Children;2022-08-26

2. Neonatal presentation of Loeys-Dietz syndrome: two case reports and review of the literature;Italian Journal of Pediatrics;2022-06-06

3. Prenatal diagnosis of ascending aortic aneurysm associated with sternal cleft;Ultrasound in Obstetrics & Gynecology;2022-02

4. Clinical and Genetic Findings in a Series of Eight Families with Arthrogryposis;Genes;2021-12-23

5. Dilated ascending aorta in the fetus;Prenatal Diagnosis;2021-07-08

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