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Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 29, 1998
A randomized controlled clinical trial on the efficacy of radiation therapy in the control of subfoveal choroidal neovascularization in age-related macular degeneration: radiation versus observationG J Bergink, C B Hoyng, R W van der Maazen, et al.
American Journal of Human Genetics|August 26, 2000
Mutations in the ABCA4 (ABCR) gene are the major cause of autosomal recessive cone-rod dystrophyA Maugeri, B J Klevering, K Rohrschneider, et al.
Neuroreport|June 7, 2000
Retinoic acid delays transcription of human retinal pigment neuroepithelium marker genes in ARPE-19 cellsJ J Janssen, E D Kuhlmann, A H van Vugt, et al.
Gene|January 13, 1998
Cloning and structural analysis of the murine GCN5L1 geneC A Driessen, H J Winkens, L D Kuhlmann, et al.
Current Eye Research|October 16, 1999
Retinoic acid receptors and retinoid X receptors in the mature retina: subtype determination and cellular distributionJ J Janssen, E D Kuhlmann, A H van Vugt, et al.
FEBS Letters|July 8, 1998
The visual cycle retinol dehydrogenase: possible involvement in the 9-cis retinoic acid biosynthetic pathwayC A Driessen, H J Winkens, E D Kuhlmann, et al.
American Journal of Ophthalmology|November 1, 1995
Ocular and systemic manifestations of cerebrotendinous xanthomatosisJ R Cruysberg, R A Wevers, B G van Engelen, et al.
Ophthalmology|July 27, 2001
Null mutation in the human 11-cis retinol dehydrogenase gene associated with fundus albipunctatusC A Driessen, B P Janssen, H J Winkens, et al.
American Journal of Medical Genetics|November 20, 1995
Clinical findings in obligate carriers of type I Usher syndromeM Wagenaar, B ter Rahe, A van Aarem, et al.
Ophthalmic Genetics|March 23, 2002
Clinical characterization, linkage analysis, and PRPC8 mutation analysis of a family with autosomal dominant retinitis pigmentosa type 13 (RP13)J J C van Lith-Verhoeven, S D van der Velde-Visser, M M Sohocki, et al.
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