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Article

Two cases of nevoid basal cell carcinoma syndrome associated with meningioma caused by a PTCH1 or SUFU germline mutation

24 Jul 2012

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 22829011
DOI: 10.1007/s10689-012-9548-0

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Two cases of nevoid basal cell carcinoma syndrome associated with meningioma caused by a PTCH1 or SUFU germline mutationPMID 22829011Read ↗

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Frameshift mutation in the PTCH2 gene can cause nevoid basal cell carcinoma syndromeSemantic proximity Read ↗

SUFU ‐associated Gorlin syndrome: Expanding the spectrum between classic nevoid basal cell carcinoma syndrome and multiple hereditary infundibulocystic basal cell carcinomaSemantic proximity Read ↗

Germline SUFU mutation carriers and medulloblastoma: clinical characteristics, cancer risk, and prognosisSemantic proximity Read ↗

A novel phenotype with features of basal cell nevus syndrome and basaloid follicular hamartoma syndrome.Semantic proximity Read ↗

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Melanoma arising in a giant congenital melanocytic nevus with neuroblastoma RAS mutation.Semantic proximity Read ↗

Genetics of the nevoid basal cell carcinoma syndrome.Semantic proximity Read ↗

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