Novel SUFU Frameshift Variant Leading to Meningioma in Three Generations in a Family with Gorlin Syndrome
Click HERE to view the article on PubMed.gov. The Gorlin Syndrome Alliance [...]
Multiple nevoid basal cell carcinoma syndrome associated with congenital orbital teratoma, caused by a PTCH1 frameshift mutation
Click HERE to view the article on PubMed.gov. The Gorlin Syndrome Alliance [...]