Genotype-phenotype correlations and differential diagnosis in autosomal dominant macular disease.
- 1 January 2001
- journal article
- review article
- Published by Springer Nature in Documenta Ophthalmologica
- Vol. 102 (3) , 197-236
- https://doi.org/10.1023/a:1017566600871
Abstract
No abstract availableKeywords
This publication has 96 references indexed in Scilit:
- Early findings in central areolar choroidal dystrophyActa Ophthalmologica, 2009
- Central areolar choroidal dystrophy and slowly progressive sensorineural hearing lossActa Ophthalmologica Scandinavica, 2009
- Pseudoinflammatory fundus dystrophy: a follow-up studyClinical Genetics, 2008
- Pattern dystrophies of the retinal pigment epitheliumActa Ophthalmologica Scandinavica, 1996
- Night blindness in Sorsby's fundus dystrophy reversed by vitamin ANature Genetics, 1995
- Retinal Degeneration slow (rds) in Mouse Results from Simple Insertion of a t Haplotype-Specific Element into Protein-Coding Exon IIGenomics, 1995
- Molecular cloning, primary structure, and orientation of the vertebrate photoreceptor cell protein peripherin in the rod outer segment disk membraneBiochemistry, 1990
- Zentrale areoläre Aderhautdystrophie mit retinalen KristallenKlinische Monatsblätter für Augenheilkunde, 1985
- Adult-onset foveomacular pigment epithelial dystrophyDocumenta Ophthalmologica, 1982
- RETINAL FUNCTIONS IN DOMINANT CYSTOID MACULAR DYSTROPHY (DCMD)Acta Ophthalmologica, 1976