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

Genetic testing without consent: the implications of the new Human Tissue Act 2004.

Journal of medical ethics - 1 Dec 2006

Lucassen A, Kaye J

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Access to Information
Share to Disclosure
Share to Ethics, Medical
Share to Genetic Predisposition to Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Privacy

Share to Genetic Testing

Share to United Kingdom

Source

Open in PubMed Open full text

Identifiers

PMID: 17145906
DOI: 10.1136/jme.2005.013631
PMCID: PMC2563345

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic testing without consent: the implications of the new Human Tissue Act 2004.PMID 17145906Read ↗

Testing for genetic traits: the need for a new legal doctrine of informed consent.Semantic proximity Read ↗

Beyond consent: ethical and social issues in genetic testingSemantic proximity Read ↗

Consent and confidentiality in clinical genetic practice: guidance on genetic testing and sharing genetic informationSemantic proximity Read ↗

Beyond the genome: the ethics of DNA testing.Semantic proximity Read ↗

Genetic testing and individual rights.Semantic proximity Read ↗

Plunging into the gene pool: even though the legal landscape has changed, concerns about the abuse of genetic testing persists.Semantic proximity Read ↗

The ethics of genetic testing: is more always better?Semantic proximity Read ↗

The meaning of human gene testing for disability rights.Semantic proximity Read ↗

Medical-ethical guidelines for genetic investigations in humans.Semantic proximity Read ↗

Ethical, legal, and social issues in genetic testing for complex genetic diseases.Semantic proximity Read ↗

23andMe, the Food and Drug Administration, and the future of genetic testing.Semantic proximity Read ↗

Genomic Testing for Human Health and Disease Across the Life Cycle: Applications and Ethical, Legal, and Social ChallengesSemantic proximity Read ↗

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