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Article

Refined genetic and physical positioning of the gene for Doyne honeycomb retinal dystrophy (DHRD).

Human genetics - 1 Jan 1999

Kermani S, Gregory-Evans K, Tarttelin E E, Bellingham J, Plant C, Bird A C, Fox M, Bhattacharya S S, Gregory-Evans C Y

Abstract excerpt

Doyne honeycomb retinal dystrophy (DHRD) is a late-onset autosomal dominant disorder that causes degeneration of the retina and can lead to blindness. We have previously assigned DHRD to a 5-cM region of chromosome 2p16 between marker loci D2S2739 and D2S378. Using sequence-tagged sites (STSs), expressed sequence tags (ESTs) and polymorphic markers within the DHRD region, we have identified 18 yeast artificial...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 10071196
DOI: 10.1007/s004390050913

Genes

STS

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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