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Boon CJF et al. - The purpose of this review is to describe this spectrum of phenotypes, which includes Best vitelliform macular dystrophy and adult-onset foveomacular vitelliform dystrophy, autosomal dominant vitreoretinochoroidopathy, the MRCS syndrome, and autosomal recessive bestrophinopathy. The genotype–phenotype correlations that are observed in association with BEST1 mutations are discussed.

Today in Basic Science/Genetics...keeping you current

Conjunctival Mucin mRNA Expression in Contact Lens Wear
Optometry and Vision Science, 12/03/09

Adding a microcomputer bar-code network to a minicomputer-based radiology information system
Journal of Digital Imaging, 12/03/09

Differences in the TGF-beta 1-induced pro-fibrotic response of anterior and posterior corneal keratocytes in vitro
Investigative Ophthalmology and Visual Science, 12/03/09