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Article

Tylosis associated with squamous cell carcinoma of the oesophagus (TOC): Report of an African family with a novel RHBDF2 variant.

Clinical genetics - 1 May 2018

Mokoena T, Smit J G M, Karusseit V O, Dorfling C M, van Rensburg E J

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Topics

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Share to Carrier Proteins
Share to Esophageal Neoplasms
Share to Esophageal Squamous Cell Carcinoma
Share to Genetic Predisposition to Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Intracellular Signaling Peptides and Proteins

Share to Keratoderma, Palmoplantar

Source

Identifiers

PMID: 29372562
DOI: 10.1111/cge.13161

Genes

RHBDF2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

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Tylosis associated with squamous cell carcinoma of the oesophagus (TOC): Report of an African family with a novel RHBDF2 variant.PMID 29372562Read ↗

Tylosis with oesophageal cancer: Diagnosis, management and molecular mechanismsSemantic proximity Read ↗

[RHBDF2 mutations in familial palmoplantar keratoderma associated with tylosis oesophageal cancer].Semantic proximity Read ↗

RHBDF2 mutations are associated with tylosis, a familial esophageal cancer syndrome.Semantic proximity Read ↗

The molecular charaterisation of the Tylosis with Oesophageal Cancer (TOC) minimal region sequenceSemantic proximity Read ↗

Novel microsatellite markers and single nucleotide polymorphisms refine the tylosis with oesophageal cancer (TOC) minimal region on 17q25 to 42.5 kb: sequencing does not identify the causative gene.Semantic proximity Read ↗

Analysis of the function of ADAM17 in iRhom2 curly-bare and tylosis with esophageal cancer mutant miceSemantic proximity Read ↗

[Palmoplantar keratosis].Semantic proximity Read ↗

Cutaneous squamous cell carcinoma in an autosomal-recessive Adams-Oliver syndrome patient with a novel frameshift pathogenic variant in the EOGT gene.Semantic proximity Read ↗

An investigation of the tylosis with oesophageal cancer (TOC) locus in Iranian patients with oesophageal squamous cell carcinoma.Semantic proximity Read ↗

Trichorhinophalangeal syndrome: Report of a novel familial TRPS1 mutation.Semantic proximity Read ↗

Abnormalities of chromosome 17 in oesophageal cancer.Semantic proximity Read ↗

Infrequent mutation of the human envoplakin gene is closely linked to the tylosis oesophageal cancer locus in sporadic oesophageal squamous cell carcinomas.Semantic proximity Read ↗

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