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Article

Milia: a useful clinical marker of CYLD mutation carrier status.

Clinical and experimental dermatology - 1 Mar 2018

Bajwa D S, Nasr B, Carmichael A J, Rajan N

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 29023940
DOI: 10.1111/ced.13296

Genes

CYLD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

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Milia: a useful clinical marker of CYLD mutation carrier status.PMID 29023940Read ↗

Phenotype–genotype correlations for clinical variants caused by CYLD mutationsSemantic proximity Read ↗

[COX7B mutations in MIDAS syndrome or microphthalmia with linear skin defects (MLS)].Semantic proximity Read ↗

Genetic Testing in CYLD Cutaneous Syndrome: An UpdateSemantic proximity Read ↗

Loss of CYLD expression unleashes Wnt signaling in multiple myeloma and is associated with aggressive diseaseSemantic proximity Read ↗

A case of Brooke-Spiegler syndrome with a new mutation in the CYLD gene.Semantic proximity Read ↗

A large family with CYLD cutaneous syndrome: medical genetics at the community levelSemantic proximity Read ↗

CYLD-related cutaneous syndrome: variable p.Pro482fs*6 phenotype in five individuals from two unrelated families.Semantic proximity Read ↗

The cylindromatosis (CYLD) gene and head and neck tumorigenesisSemantic proximity Read ↗

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

New mutation in the CYLD gene within a family with Brooke-Spiegler syndrome.Semantic proximity Read ↗

Cylindromatosis and the <i>CYLD</i> gene: new lessons on the molecular principles of epithelial growth controlSemantic proximity Read ↗

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

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