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

Extending the p16-Leiden tumour spectrum by respiratory tract tumours.

Journal of medical genetics - 1 Mar 2004

Oldenburg R A, de Vos tot Nederveen Cappel W H, van Puijenbroek M, van den Ouweland A, Bakker E, Griffioen G, Devilee P, Cornelisse C J, Meijers-Heijboer H, Vasen H F A, Morreau H

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 Carcinoma, Squamous Cell
Share to Cyclin-Dependent Kinase Inhibitor p16
Share to Digestive System Neoplasms

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genes, p16

Share to Germ-Line Mutation

Share to Loss of Heterozygosity

Share to Melanoma

Share to Mouth Neoplasms

Source

Open in PubMed Open full text

Identifiers

PMID: 14985402
DOI: 10.1136/jmg.2003.012336
PMCID: PMC1735708

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Extending the p16-Leiden tumour spectrum by respiratory tract tumours.PMID 14985402Read ↗

WHO Classification of Tumours: Pathology and Genetics. Tumours of Haematopoietic and Lymphoid TissuesSemantic proximity Read ↗

[Pathology and genetics of disease and tumours of the lung, pleura in China].Semantic proximity Read ↗

Defining and refining the phenotype of PRRT2 mutations.Semantic proximity Read ↗

SCL19A3 gene mutation with Leigh-like phenotype presentation: a potentially treatable disease.Semantic proximity Read ↗

A genetic view of laryngeal cancer heterogeneity.Semantic proximity Read ↗

Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor PhenotypeSemantic proximity Read ↗

[Secondary malignant neoplasms].Semantic proximity Read ↗

Pleural fluid overload-associated large B-cell lymphoma with a formerly double-hit genotype.Semantic proximity Read ↗

Lung disease in FLNA mutation: Confirmatory reportSemantic proximity Read ↗

NTHL1-associate polyposis: first Australian case reportSemantic proximity Read ↗

Leukaemia Research Fund annual guest lecture 1990. Genetics lesions in preleukaemia.Semantic proximity Read ↗

RB1-deficient squamous cell carcinoma: the proposed source of combined Merkel cell carcinomaSemantic proximity Read ↗

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