Novel Fibrillin 1 Mutation in a Case of Neonatal Marfan Syndrome: The Increasing Importance of Early Recognition-Reference-Cited by-同舟云学术

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Novel Fibrillin 1 Mutation in a Case of Neonatal Marfan Syndrome: The Increasing Importance of Early Recognition

Published:2007-09 Issue:5 Volume:2 Page:342-346
ISSN:1747-079X
Container-title:Congenital Heart Disease
language:en
Short-container-title:Congenital Heart Disease

Author:

Sutherell Jamie,Zarate Yuri,Tinkle Bradley T.,Markham Larry W.,Cripe Linda H.,Hyland James C.,Witte David,Hopkin Robert J.,Hinton Robert B.

Publisher

Computers, Materials and Continua (Tech Science Press)

Subject

Cardiology and Cardiovascular Medicine,Radiology, Nuclear Medicine and imaging,General Medicine,Surgery,Pediatrics, Perinatology and Child Health

Reference17 articles.

1. Marfan's syndrome

2. Comprehensive molecular screening of theFBN1gene favors locus homogeneity of classical Marfan syndrome

3. The molecular genetics of Marfan syndrome and related disorders

Cited by 16 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. Genotype-phenotype spectrum and prognosis of early-onset Marfan syndrome;BMC Pediatrics;2023-10-28

2. Health Supervision for Children and Adolescents With Marfan Syndrome;Pediatrics;2023-03-20

3. A novel large in-frame FBN1 deletion causes neonatal Marfan syndrome;CSH MOL CASE STUD;2022

4. Neonatal Marfan syndrome with missense variant of c.3706T>C undergoing bilateral atrioventricular valve replacement;Cardiology in the Young;2021-09-16

5. Neonatal Marfan Syndrome by Inherited Mutation;The Indian Journal of Pediatrics;2020-06-17

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