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

Hereditary p16-Leiden mutation in a patient with multiple head and neck tumors.

American journal of human genetics - 1 Jan 2003

Schneider-Stock Regine, Giers Anja, Motsch Christiane, Boltze Carsten, Evert Matthias, Freigang Bernd, Roessner Albert

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 DNA Methylation
Share to Gene Deletion
Share to Genes, p16
Share to Head and Neck Neoplasms

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

Share to Heterozygote

Share to Mutation

Source

Open in PubMed Open full text

Identifiers

PMID: 12549483
DOI: 10.1086/345397
PMCID: PMC378629

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 · 8 closest

Hereditary p16-Leiden mutation in a patient with multiple head and neck tumors.PMID 12549483Read ↗

Extending the p16-Leiden tumour spectrum by respiratory tract tumours.Semantic proximity Read ↗

Common Germline Mutations in a Patient With Multiple Primary Lung Cancers.Semantic proximity Read ↗

[Biallelic inactivation of the p16-Gen in a metachronous triple carcinoma in the oropharyngeal region].Semantic proximity Read ↗

Multiple melanomas after treatment for Hodgkin lymphoma in a non-Dutch p16-Leiden mutation carrier with 2 MC1R high-risk variants.Semantic proximity Read ↗

Increased risk of larynx cancer in heterozygous carriers of the I171V mutation of the NBS1 gene.Semantic proximity Read ↗

Multiple squamous cell carcinomas of the head and neck show different phenotypes of allelic loss patterns suggesting different clonal origin of carcinogenesis.Semantic proximity Read ↗

Proptosis in a family with the p16 Leuc-to-Prol mutation in the PMP22 gene (CMT 1E).Semantic proximity Read ↗

Second-hit APC mutation in a familial adamantinomatous craniopharyngioma.Semantic proximity Read ↗

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