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Article

Spectrum of PTCH1 Mutations in French Patients with Gorlin Syndrome

19 Aug 2003

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 12925203
DOI: 10.1046/j.1523-1747.2003.12423.x

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Spectrum of PTCH1 Mutations in French Patients with Gorlin SyndromePMID 12925203Read ↗

Novel mutation in the PTCH1 gene in a patient with Gorlin syndrome with prominent clinical features.Semantic proximity Read ↗

A novel PTCH1 mutation in a patient with Gorlin syndromeSemantic proximity Read ↗

Novel PTCH1 Mutation in a Young Child With Gorlin Syndrome and Medulloblastoma.Semantic proximity Read ↗

Novel PTCH1 mutation in Gorlin-Goltz syndrome potentially altered interactions with lipid bilayer.Semantic proximity Read ↗

Gorlin-like phenotype in a patient with a PTCH2 variant of uncertain significance.Semantic proximity Read ↗

Novel PTCH1 Mutation Causes Gorlin-Goltz Syndrome.Semantic proximity Read ↗

Genetic Analysis of Gorlin Syndrome Using a Multiplex PCR Gene Panel, and Its Potential Clinical Utility for Liquid BiopsySemantic proximity Read ↗

Development of a targeted gene panel for the diagnosis of Gorlin syndrome.Semantic proximity Read ↗

Current recommendations for cancer surveillance in Gorlin syndrome: a report from the SIOPE host genome working group (SIOPE HGWG)Semantic proximity Read ↗

Intronic splicing mutations in PTCH1 cause Gorlin syndrome.Semantic proximity Read ↗

PTCH2 is not a strong candidate gene for gorlin syndrome predisposition.Semantic proximity Read ↗

Molecular characterization of Italian nevoid basal cell carcinoma syndrome patients.Semantic proximity Read ↗

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