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Article

Localisation of a gene for dominant cone-rod dystrophy (CORD6) to chromosome 17p.

Human molecular genetics - 1 Apr 1997

Kelsell R E, Evans K, Gregory C Y, Moore A T, Bird A C, Hunt D M

Abstract excerpt

We have performed genetic linkage analysis on a four generation British family with cone-rod dystrophy. Significant linkage to the disease gene was obtained with eight marker loci situated on chromosome 17p12-p13. A maximum two-point lod score of 5.93 with no recombination was obtained with marke...

Topics

Chromosome Mapping
Chromosomes, Human, Pair 17
Female
Genes, Dominant
Genetic Linkage
Genetic Markers
Genotype
Humans
Lod Score
Male
Microsatellite Repeats
Mutation
Pedigree

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Phenotype

Recombination, Genetic

Retinitis Pigmentosa

United Kingdom

Source

Identifiers

PMID: 9097965
DOI: 10.1093/hmg/6.4.597

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-9097965-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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