Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Exploring the dense mapping of a region of potential linkage in complex disease: an example in multiple sclerosis.

Genetic epidemiology - 1 Jan 1999

Feakes R, Sawcer S, Chataway J, Coraddu F, Broadley S, Gray J, Jones H B, Clayton D, Goodfellow P N, Compston A

Abstract excerpt

In 1996 we reported the results of a genome screen in multiple sclerosis, in which potential linkage was identified in a total of twenty regions, including the centromeric region of chromosome 5. In order to investigate the efficiency of typing dense arrays of markers in regions of potential linkage, we have typed an additional nineteen microsatellite markers from this chromosome 5 region (D5S623 - D5S428) in the...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Chromosome Mapping
Share to Chromosomes, Human, Pair 5

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

Share to Genetic Linkage

Share to Genetic Markers

Share to Genotype

Share to Linkage Disequilibrium

Share to Microsatellite Repeats

Share to Multiple Sclerosis

Source

Identifiers

PMID: 10323184
DOI: 10.1002/(SICI)1098-2272(1999)17:1<51::AID-GEPI4>3.0.CO;2-V

Provenance

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.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Exploring the dense mapping of a region of potential linkage in complex disease: an example in multiple sclerosis.PMID 10323184Read ↗

A high-density screen for linkage in multiple sclerosis.Semantic proximity Read ↗

Enhancing linkage analysis of complex disorders: an evaluation of high-density genotyping.Semantic proximity Read ↗

Refining the linkage analysis on chromosome 10 in 449 sib-pairs with multiple sclerosis.Semantic proximity Read ↗

A meta-analysis of whole genome linkage screens in multiple sclerosis.Semantic proximity Read ↗

Investigation of seven proposed regions of linkage in multiple sclerosis: an American and French collaborative study.Semantic proximity Read ↗

Updated results of the United Kingdom linkage-based genome screen in multiple sclerosis.Semantic proximity Read ↗

Identification by denaturing high-performance liquid chromatography of numerous polymorphisms in a candidate region for multiple sclerosis susceptibility.Semantic proximity Read ↗

Progress towards completing the human linkage map.Semantic proximity Read ↗

A genome screen for linkage disequilibrium in Turkish multiple sclerosis.Semantic proximity Read ↗

Assessing accuracy in linkage analysis by means of confidence regions.Semantic proximity Read ↗

Fine mapping of the multiple sclerosis susceptibility locus on 5p14-p12.Semantic proximity Read ↗

Genetic refinement of the chromosome 5q lattice corneal dystrophy type I locus to within a 2 cM interval.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.