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See Latest ArticlesGenotyping microarray for CSNB-associated genes
Investigative Ophthalmology and Visual Science, 07/08/09
Zeitz C et al. - This relatively inexpensive first-pass genetic testing device for patients diagnosed with CSNB will improve molecular diagnostics and genetic counselling of patients and their families and gives the opportunity to analyse if for example more progressive disorders like cone or cone-rod dystrophies also underlie the same gene defects.
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Comparison of High-Resolution Melting Analysis with denaturing High-Performance Liquid Chromatography for Mutation Scanning in the ABCA4 gene
Investigative Ophthalmology and Visual Science, 12/09/09
A homozygous p.Glu150Lys mutation in the opsin gene of two Pakistani families with autosomal recessive retinitis pigmentosa
Molecular Vision, 12/08/09
Today in Low Vision...keeping you current
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Corneal and Refractive Astigmatism in Adults: A Power Vectors Analysis
Optometry and Vision Science, 12/09/09
Academic Behaviors in Children with Convergence Insufficiency with and without Parent-Reported ADHD
Optometry and Vision Science, 12/09/09
Rasch Analysis of Visual Function and Quality of Life Questionnaires
Optometry and Vision Science, 12/09/09
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