Patched homolog 1 gene mutation (p.G1093R) induces nevoid basal cell carcinoma syndrome and non-syndromic keratocystic odontogenic tumors: A case report-Reference-Cited by-同舟云学术

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Patched homolog 1 gene mutation (p.G1093R) induces nevoid basal cell carcinoma syndrome and non-syndromic keratocystic odontogenic tumors: A case report

Published:2012-05-08 Issue:2 Volume:4 Page:241-244
ISSN:1792-1074
Container-title:Oncology Letters
language:en
Short-container-title:

Author:

PONTI GIOVANNI,POLLIO ANNAMARIA,PASTORINO LORENZA,PELLACANI GIOVANNI,MAGNONI CRISTINA,NASTI SABINA,FORTUNA GIULIO,TOMASI ALDO,SCARRÀ GIOVANNA BIANCHI,SEIDENARI STEFANIA

Publisher

Spandidos Publications

Subject

Cancer Research,Oncology

Cited by 8 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. PTCH1 Germline Mutations and the Basaloid Follicular Hamartoma Values in the Tumor Spectrum of Basal Cell Carcinoma Syndrome (NBCCS);Anticancer Research;2018-01-02

2. Use of anteromedial thigh perforator flap and immunological implications of Gorlin-Goltz syndrome: a case study;Journal of Wound Care;2016-12-02

3. Skeletal stigmata as keys to access to the composite and ancient Gorlin–Goltz syndrome history: The Egypt, Pompeii and Herculaneum lessons;Gene;2016-09

4. Molecular Signaling in Benign Odontogenic Neoplasia Pathogenesis;Current Oral Health Reports;2016-03-31

5. Skeletal and cranio-facial signs in Gorlin syndrome from ancient Egypt to the modern age: sphenoid asymmetry in a patient with a novel PTCH1 mutation;Future Oncology;2014-05

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