Concepedia

Evidence of Genetic Heterogeneity in MRCS (Microcornea, Rod-Cone Dystrophy, Cataract, and Posterior Staphyloma) Syndrome

Michel Michaelides, Jill Urquhart, Graham E. Holder, Marie Restori, Nuha Kayali, Forbes Manson, Graeme C. Black

American Journal of Ophthalmology · 2006 · 28 citations · 3 references

DOI

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3

Mutations of <i>VMD2</i> Splicing Regulators Cause Nanophthalmos and Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC)

Jill Yardley, Bart P. Leroy, Niki Hart‐Holden et al. · Investigative Ophthalmology & Visual Science · 2004 · 228 citations · Full text

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Ten novel mutations in<i>VMD2</i>associated with Best macular dystrophy (BMD)

Franziska Krämer, Nicole Mohr, Ulrich Kellner et al. · Human Mutation · 2003 · 68 citations

, , +14

A clinical and molecular genetic study of a rare dominantly inherited syndrome (MRCS) comprising of microcornea, rod-cone dystrophy, cataract, and posterior staphyloma

M. Ashwin Reddy · British Journal of Ophthalmology · 2003 · 46 citations · Full text

, , +14