Genetic Evaluation to Establish the Diagnosis of X-Linked Familial Exudative Vitreoretinopathy
Author:
Publisher
Informa UK Limited
Subject
Genetics(clinical),Ophthalmology,Pediatrics, Perinatology, and Child Health
Link
http://www.tandfonline.com/doi/pdf/10.1080/13816810600862402
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1. Vascular Development in the Retina and Inner Ear
2. Astrocyte–Endothelial Cell Relationships during Human Retinal Vascular Development
3. Phenotypic heterogeneity associated with a novel mutation (Gly112Glu) in the Norrie disease protein
4. Mutations in LRP5 or FZD4 Underlie the Common Familial Exudative Vitreoretinopathy Locus on Chromosome 11q
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