Documentation of anomalies not previously described in Fryns syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference35 articles.
1. Congenital diaphragmatic hernia, coarse facies, and acral hypoplasia: Fryns syndrome
2. Fryns syndrome: two further cases without lateral diaphragmatic defects
3. Pulmonary agenesis, microphthalmia, and diaphragmatic defect (PMD): New syndrome or association?
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1. Clinical and mutation analysis of 51 probands with anophthalmia and/or severe microphthalmia from a single center;Molecular Genetics & Genomic Medicine;2013-03-27
2. Fryns Syndrome in Monozygotic Twins: A Case Report with Review of Literature;International Journal of Morphology;2012-03
3. Congenital Defects of the Abdominal Wall;Pediatric Surgery;2012
4. Fetal Gastrointestinal Abnormalities;High Risk Pregnancy;2011
5. Syndromes and Disorders Associated with Omphalocele (III): Single Gene Disorders, Neural Tube Defects, Diaphragmatic Defects and Others;Taiwanese Journal of Obstetrics and Gynecology;2007-06
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