M P Snead, D K Newmann, A Poulson, J D Scott. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Eye Diseases/geneticsGenes, DominantHumansRetinal Diseases/geneticsSyndromeVitreous Body
Year: 1995 PMID: 8626092 DOI: 10.1007/bf00184095
Source DB: PubMed Journal: Graefes Arch Clin Exp Ophthalmol ISSN: 0721-832X Impact factor: 3.117