Fryns Syndrome: A Lethal Birth Defect with Variable Phenotypic Expressions in Siblings-Reference-Cited by-同舟云学术

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Fryns Syndrome: A Lethal Birth Defect with Variable Phenotypic Expressions in Siblings

Published:2013-04-19 Issue:6 Volume:81 Page:614-616
ISSN:0019-5456
Container-title:The Indian Journal of Pediatrics
language:en
Short-container-title:Indian J Pediatr

Author:

Arora Kamaldeep,Thukral Anu,Das Rashmi Ranjan,Gupta Neerja,Kabra Madhulika,Agarwal Ramesh

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s12098-013-1011-1.pdf

Reference10 articles.

1. Fryns JP. Fryns syndrome: A variable MCA syndrome with diaphragmatic defects, coarse face, and distal limb hypoplasia. J Med Genet. 1987;24:271–4.

2. Aymé S, Julian C, Gambarelli D, et al. Fryns syndrome: Report on 8 new cases. Clin Genet. 1989;35:191–201.

3. Dillon E, Renwick M. Antenatal detection of congenital diaphragmatic hernias: The Northern region experience. Clin Radiol. 1993;48:264–7.

4. Slavotinek AM. Fryns syndrome: A review of the phenotype and diagnostic guidelines. Am J Med Genet. 2004;124A:427–33.

5. Alessandri L, Brayer C, Attali T, et al. Fryns syndrome without diaphragmatic hernia. Report on a new case and review of the literature. Genet Couns. 2005;16:363–70.

Cited by 2 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. The Genetics of Facial Cleft;Prenatal Diagnosis of Orofacial Malformations;2017

2. Prenatal and postnatal findings in five cases of Fryns syndrome;Prenatal Diagnosis;2014-07-22

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