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

Frequencies of the hereditary hemochromatosis allele in different populations. Comparison of previous phenotypic methods and novel genotypic methods.

International journal of hematology - 1 Jan 2003

Milman Nils, Pedersen Palle, Steig Torkil á, Melsen Gitte Vedel

Abstract excerpt

AIM: The frequencies of the hereditary hemochromatosis allele were compared for different populations assessed by previous phenotypic methods and the present genotypic methods. METHODS: From a literature survey, the calculated hemochromatosis allele frequencies from 16 studies using phenotypic biochemical markers (threshold levels for transferrin saturation [range, 46%-70%] and serum ferritin [range, 164-700...

Read the complete abstract on PubMed

Topics

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

Share to Biomarkers
Share to Ferritins

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

Share to Gene Frequency

Share to Genotype

Share to Hemochromatosis

Share to Mass Screening

Share to Population

Share to Transferrin

Source

Identifiers

PMID: 12568299
DOI: 10.1007/BF02982602

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

Frequencies of the hereditary hemochromatosis allele in different populations. Comparison of previous phenotypic methods and novel genotypic methods.PMID 12568299Read ↗

The Southern French registry of genetic hemochromatosis: a tool for determining clinical prevalence of the disorder and genotype penetrance.Semantic proximity Read ↗

Therapeutic recommendations in HFE hemochromatosis for p.Cys282Tyr (C282Y/C282Y) homozygous genotypeSemantic proximity Read ↗

Hemochromatosis genotypes and risk of iron overload--a meta-analysis.Semantic proximity Read ↗

Hereditary hemochromatosis: population screening based on phenotype in Brazilian blood donors.Semantic proximity Read ↗

Frequency and biochemical expression of C282Y/H63D hemochromatosis (HFE) gene mutations in the healthy adult population in Italy.Semantic proximity Read ↗

Hemochromatosis gene HFE Cys282Tyr mutation analysis in a cohort of Northeast German hospitalized patients supports assumption of a North to South allele frequency gradient throughout Germany.Semantic proximity Read ↗

[Hereditary hemochromatosis: phenotypic study in a Spanish population].Semantic proximity Read ↗

Population screening for haemochromatosis: expectations based on a study of relatives of symptomatic probands.Semantic proximity Read ↗

Correlation of Genotype and Phenotype in 32 Patients with Hereditary Hemochromatosis in ChinaSemantic proximity Read ↗

Genotype screening for hereditary hemochromatosis among voluntary blood donors in Hungary.Semantic proximity Read ↗

Genotypic/phenotypic correlations in genetic hemochromatosis: evolution of diagnostic criteria.Semantic proximity Read ↗

Hemochromatosis in a Lithuanian with HFE C282Y homozygosity and C282Y allele frequencies in the Baltic Sea region.Semantic proximity Read ↗

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