FEVR phenotype associated with septo-optic dysplasia-Reference-Cited by-同舟云学术

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FEVR phenotype associated with septo-optic dysplasia

Published:2019-09-03 Issue:5 Volume:40 Page:449-452
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Zhang David L.¹^ORCID,Blair Michael P.¹²,Zeid Janice L.³,Basith Syeda S.T.³,Shapiro Michael J.¹

Affiliation:

1. Retina Consultants Ltd., Des Plaines, Illinois, USA

2. Department of Ophthalmology and Visual Science, University of Chicago, Chicago, Illinois, USA

3. Department of Pediatric Ophthalmology, Ann & Robert H. Lurie Children’s Hospital of Chicago, Chicago, Illinois, USA

Publisher

Informa UK Limited

Subject

Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/13816810.2019.1660380

Reference22 articles.

1. Septo-optic dysplasia

2. Familial Exudative Vitreoretinopathy

3. A mutation in the Norrie disease gene (NDP) associated with X–linked familial exudative vitreoretinopathy

4. Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy

5. Mutations in LRP5 or FZD4 Underlie the Common Familial Exudative Vitreoretinopathy Locus on Chromosome 11q

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. Peripheral Retinal Nonperfusion in Pediatric Patients with Optic Disc Hypoplasia;American Journal of Ophthalmology;2023-08

2. Novel Exon 7 Deletions in TSPAN12 in a Three-Generation FEVR Family: A Case Report and Literature Review;Genes;2023-02-25

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