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Keywords: PTCH1
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Journal Articles

Gorlin Syndrome Patient with Large Deletion in 9q22.32–q22.33 Detected by Quantitative Multiplex Fluorescent PCR

Available to Purchase
Subject Area:
Dermatology , Immunology and Allergy
Vesna Musani, Maja Cretnik, Mirna Situm, Aleksandra Basta-Juzbasic, Sonja Levanat
Journal: Dermatology
Dermatology (2009) 219 (2): 111–118.
https://doi.org/10.1159/000219247
Published Online: 14 May 2009
...Vesna Musani; Maja Cretnik; Mirna Situm; Aleksandra Basta-Juzbasic; Sonja Levanat Background: Gorlin syndrome is a rare autosomal-dominant disorder characterized by a wide range of developmental abnormalities and various tumors. The syndrome is caused by mutations in PTCH1 , a tumor suppressor gene...
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