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

The frequency of the haemochromatosis-associated genotype D6S265-1:D6S105-8 in blood donors.

British journal of haematology - 1 Jun 1996

Worwood M, Dorak M T, Nicklin S, Stone C, Pointon J, Darke C

Abstract excerpt

Homozygosity for HLA-A3 and the microsatellite markers D6S265 allele 1 and D6S105 allele 8 is associated with a high relative risk for genetic haemochromatosis-indeed we and others have suggested that a haplotype including D6S265-1, HLA-A3 and D6S105-8 is specific for haemochromatosis. To determine the frequency of this haplotype and examine its specificity for haemochromatosis we have analysed data from 7820...

Read the complete abstract on PubMed

Topics

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

Share to Aged
Share to Blood Donors
Share to Gene Frequency

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

Share to Genotype

Share to Hemochromatosis

Share to HLA-A3 Antigen

Share to Homozygote

Share to Microsatellite Repeats

Source

Identifiers

PMID: 8703814
DOI: 10.1046/j.1365-2141.1996.d01-1732.x

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

The frequency of the haemochromatosis-associated genotype D6S265-1:D6S105-8 in blood donors.PMID 8703814Read ↗

Alleles at D6S265 and D6S105 define a haemochromatosis-specific genotype.Semantic proximity Read ↗

The frequency of hemochromatosis-associated alleles is increased in British patients with sporadic porphyria cutanea tarda.Semantic proximity Read ↗

Distribution of alleles at D6S105 and D6S265 with possible HLA haplotype associations.Semantic proximity Read ↗

Prevalence of HLA-DQA1 alleles and haplotypes in blood donors resident in Wales.Semantic proximity Read ↗

Allelic association of microsatellites of 6p in Italian hemochromatosis patients.Semantic proximity Read ↗

A high prevalence of HLA-H 845A mutations in hemochromatosis patients and the normal population in eastern England.Semantic proximity Read ↗

HLA class I (A, B) and II (DR, DQ) gene and haplotype frequencies in blood donors from Wales.Semantic proximity Read ↗

Haplotype analysis in Australian hemochromatosis patients: evidence for a predominant ancestral haplotype exclusively associated with hemochromatosis.Semantic proximity Read ↗

Allelic associations and homozygosity at loci from HLA-B to D6S299 in genetic haemochromatosis.Semantic proximity Read ↗

New polymorphic microsatellite markers place the haemochromatosis gene telomeric to D6S105.Semantic proximity Read ↗

A putative gene located at the MHC class I region around the D6S105 marker contributes to the setting of CD8+ T-lymphocyte numbers in humans.Semantic proximity Read ↗

A candidate gene for hemochromatosis: frequency of the C282Y and H63D mutations.Semantic proximity Read ↗

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