1-2 of 2
Keywords: Gorlin syndrome
Close
Follow your search
Access your saved searches in your account

Would you like to receive an alert when new items match your search?
Close Modal
Sort by
Journal Articles
Journal: Dermatology
Dermatology (2016) 232 (Suppl. 1): 29–31.
Published Online: 11 August 2016
...Marco Stieger; Robert E. Hunger Background: Gorlin syndrome, also known as the basal cell nevus syndrome (OMIM #109400), is a rare autosomal-dominant genetic disease. The disease, which shows mutation of the patched receptor gene ( PTCH1 ) of the sonic hedgehog pathway, is characterized...
Journal Articles
Journal: Dermatology
Dermatology (2009) 219 (2): 111–118.
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...