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Article

Familial cylindromatosis (turban tumour syndrome) gene localised to chromosome 16q12–q13: evidence for its role as a tumour suppressor gene

1 Dec 1995

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Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 7493027
DOI: 10.1038/ng1295-441

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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

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Familial cylindromatosis (turban tumour syndrome) gene localised to chromosome 16q12–q13: evidence for its role as a tumour suppressor genePMID 7493027Read ↗

Familial cylindromatosis and brooke-spiegler syndrome: a review of current therapeutic approaches and the surgical challenges posed by two affected families.Semantic proximity Read ↗

Phenotype diversity in familial cylindromatosis: a frameshift mutation in the tumor suppressor gene CYLD underlies different tumors of skin appendages.Semantic proximity Read ↗

Linkage and LOH studies in 19 cylindromatosis families show no evidence of genetic heterogeneity and refine the CYLD locus on chromosome 16q12-q13.Semantic proximity Read ↗

Molecular Analysis of Chromosome 16q Regions in Dermal Analogue Tumors of Salivary GlandsSemantic proximity Read ↗

A new hereditary cylindromatosis family associated with CYLD1 on chromosome 16.Semantic proximity Read ↗

Inherited cylindromas: lessons from a rare tumour.Semantic proximity Read ↗

Understanding Inherited Cylindromas: Clinical Implications of Gene Discovery.Semantic proximity Read ↗

Identification of the familial cylindromatosis tumour-suppressor gene.Semantic proximity Read ↗

Mild phenotype of familial cylindromatosis associated with an R758X nonsense mutation in the CYLD tumour suppressor gene.Semantic proximity Read ↗

Multiple Familial Trichoepithelioma Caused by Mutations in the Cylindromatosis Tumor Suppressor GeneSemantic proximity Read ↗

A mutational hotspot in CYLD causing cylindromas: a comparison of phenotypes arising in different genetic backgrounds.Semantic proximity Read ↗

Diverse phenotype of Brooke-Spiegler syndrome associated with a nonsense mutation in the CYLD tumor suppressor gene.Semantic proximity Read ↗

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