Congenital diaphragmatic hernia, coarse facies, and acral hypoplasia: Fryns syndrome-Reference-Cited by-同舟云学术

Congenital diaphragmatic hernia, coarse facies, and acral hypoplasia: Fryns syndrome

Published:1989-01 Issue:1 Volume:32 Page:93-99
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Bamforth J. Stephen,Leonard Claire O.,Chodirker Bernard N.,Chitayat David,Gritter Hilda L.,Evans Jane A.,Keena Beth,Pantzar Tapio,Friedman Jan M.,Hall Judith G.,Opitz John M.,Reynolds James F.

Publisher

Wiley

Subject

Genetics (clinical)

Reference15 articles.

1. Empirical recurrence risk after unidentified multiple congenital abnormalities.

2. Absent left hemidiaphragm, arhinencephaly, and cardiac malformations.

3. (1986): “Genetic Causes of Mental Retardation. A Personal Contribution.” pp 336. Leuven: Katholieke Universiteit.

4. A new lethal syndrome with cloudy corneae, diaphragmatic defects and distal limb deformities

Cited by 57 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. Association of concomitant congenital diaphragmatic hernia and Hirschsprung's disease with a mutation in the FOXP1 gene: A case report;Journal of Pediatric Surgery Case Reports;2024-07

2. When Fryn met Edward: Two rare syndromes in a single patient;Medical Journal Armed Forces India;2022-01

3. Concurrent Morgagni and Bochdalek congenital diaphragmatic hernias with omphalocele;Journal of Pediatric Surgery Case Reports;2021-07

4. Diaphragmatic Hernia as a Prenatal Feature of Glycosylphosphatidylinositol Biosynthesis Defects and the Overlap With Fryns Syndrome – Literature Review;Frontiers in Genetics;2021-06-07

5. Variable expression pattern in Donnai-Barrow syndrome: Report of two novel LRP2 mutations and review of the literature;European Journal of Medical Genetics;2015-05