Bech, Niels

Fingert, John H

Johnsen, Thorkild

Larsen, Michael

Roos, Ben

Rosenberg, Thomas

Scheetz, Todd E

Stone, Edwin M

English

PubMed

Copenhagen University Research Information System

Clinical and genetic characterization of a Danish family with North Carolina macular dystrophy

A Korean family with an early-onset autosomal dominant macular dystrophy resembling North Carolina macular dystrophy.

A New dominant Progressive Foveal Dystrophy.

A North Carolina macular dystrophy phenotype in a Belizean family maps to the MCDR1 locus.

A Reappraisal of the Clinical Spectrum of North Carolina Macular Dystrophy. Ophthalmology

An early-onset autosomal dominant macular dystrophy (MCDR3) resembling North Carolina macular dystrophy maps to chromosome 5. Invest Ophthalmol Vis Sci 2003:2178-83. [PMID:

Avoiding recomputation in linkage analysis. Hum Hered

Carolina macular dystrophy phenotype in France maps to the MCDR1 locus. Mol Vis

Carolina's dominant progressive foveal dystrophy: how progressive is it?

Central areolar pigment epithelial dystrophy. Ophthalmologica

Clinical and genetic evidence for autosomal dominant North Carolina macular dystrophy in a German family.

Clinical characterization and genetic mapping of North Carolina macular dystrophy. Vision Res

Clinical spectrum of chromosome 6-linked autosomal dominant drusen and macular degeneration.

Comprehensive functional vision assessment of patients with North Carolina macular dystrophy (MCDR1). Retina

Correlation of fundus autofluorescence with photoreceptor morphology and functional changes in eyes with retinitis pigmentosa. Acta Ophthalmol 2010; 88:e177-83. [PMID: 20491687] Molecular Vision 2010; 16:2659-2668 ©

Easy calculations of lod scores and genetic risks on small computers.

easyLINKAGE-Plus–automated linkage analyses using large-scale SNP data. Bioinformatics

Fast and sensitive silver staining of DNA in polyacrylamide gels. Anal Biochem

Faster sequential genetic linkage computations.

Genetic linkage analysis of a novel syndrome comprising North Carolina-like macular dystrophy and progressive sensorineural hearing loss.

Histopathology of incipient fundus flavimaculatus. Ophthalmology

Imaging of retinal autofluorescence in patients with age-related macular degeneration. Retina

LeflerWHWadsworthJACSidburyJBHereditary macular degeneration and amino-aciduria.Am

Macular function testing in a German pedigree with North Carolina macular dystrophy. Retina

North Carolina macular dystrophy (MCDR1) locus: a fine resolution genetic map and haplotype analysis.

North Carolina macular dystrophy and central areolar pigment epithelial dystrophy. One family, one disease. Arch Ophthalmol

North Carolina macular dystrophy is assigned to chromosome 6. Genomics

North Carolina Macular Dystrophy, Revisted. Ophthalmology

North Carolina macular dystrophy: clinical features, genealogy, and genetic linkage analysis. Trans Am Ophthalmol Soc

North Carolina macular dystrophy: clinicopathologic correlation.

North Carolina macular dystrophy: clinicopathologic correlation. Trans Am Ophthalmol Soc

North Carolina Macular Dystrophy: Exclusion Map Using RFLPs and Microsatellites. Genomics

Phenotype of a British North Carolina macular dystrophy family linked to chromosome 6q.

Standard for clinical electroretinography

http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=3002954

Clinical and genetic characterization of a Danish family with North Carolina macular dystrophy

Abstract

Similar works

Full text

Available Versions

Copenhagen University Research Information System