A novel PTCH1 gene mutation in a pediatric patient associated multiple keratocystic odontogenic tumors of the jaws and Gorlin

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A novel PTCH1 gene mutation in a pediatric patient associated multiple keratocystic odontogenic tumors of the jaws and Gorlin–Goltz syndrome

Published:2016 Issue:3 Volume:59 Page:335
ISSN:0377-4929
Container-title:Indian Journal of Pathology and Microbiology
language:en
Short-container-title:Indian J Pathol Microbiol

Author:

Ozcan Gozde,Balta Burhan,Sekerci AhmetErcan,Etoz OsmanA,Martinuzzi Claudia,Kara Ozlem,Pastorino Lorenza,Kocoglu Fatma,Ulker Omer,Erdogan Murat

Publisher

Medknow

Subject

Microbiology (medical),General Medicine,Pathology and Forensic Medicine

Cited by 3 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. Radiological evaluation of odontogenic keratocysts in patients with nevoid basal cell carcinoma syndrome: A review;The Saudi Dental Journal;2023-09

2. Gorlin-Goltz syndrome with familial manifestation;Biomedical Papers;2021-02-04

3. Molecular Genetics of Basal Cell Naevus Syndrome;eLS;2018-03-30

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