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 prioritisation of genetic screening with primary haemochromatosis as an example].

Nederlands tijdschrift voor geneeskunde - 26 Jul 2003

de Craen A J, van Aken M O, Westendorp R G

Abstract excerpt

In 1994, the Health Council of the Netherlands published a report entitled 'Genetic screening' which contained 12 criteria for genetic screening programmes. However, the list does not prioritize the various criteria. From the list we have selected two criteria that we consider to be the most impo...

Read the complete abstract on PubMed

Topics

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

Share to Diagnosis, Differential
Share to Genetic Markers
Share to Genetic Predisposition to Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Testing

Share to Hemochromatosis

Source

Identifiers

PMID: 12908344

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-12908344-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 10 closest

[The prioritisation of genetic screening with primary haemochromatosis as an example].PMID 12908344Read ↗

[Hemochromatosis: the importance of mutation screening in the family].Semantic proximity Read ↗

[Should we support large-scale screening for genetic haemochromatosis in France?].Semantic proximity Read ↗

Screening for hemochromatosis.Semantic proximity Read ↗

[Value of genetic diagnosis of C282Y mutation in patients with hereditary hemochromatosis].Semantic proximity Read ↗

Strategies for early diagnosis of haemochromatosis.Semantic proximity Read ↗

[Screening for hereditary HFE hemochromatosis].Semantic proximity Read ↗

Is genetic screening for hemochromatosis worthwhile?Semantic proximity Read ↗

Gender-specific phenotypic expression and screening strategies in C282Y-linked haemochromatosis: a study of 9396 French people.Semantic proximity Read ↗

A rare case of a patient heterozygous for the hemochromatosis mutation C282Y and homozygous for H63D.Semantic proximity Read ↗

Factors affecting the uptake of screening: a randomised controlled non-inferiority trial comparing a genotypic and a phenotypic strategy for screening for haemochromatosis.Semantic proximity Read ↗

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