Novel mutation in PTCH1 gene in a patient with basal cell nevus syndrome and uterus bicornisRead More
Novel SUFU Frameshift Variant Leading to Meningioma in Three Generations in a Family with Gorlin SyndromeRead More
Lack of genotype-phenotype correlation in basal cell nevus syndrome: A Dutch multicenter retrospective cohort studyRead More
Multiple nevoid basal cell carcinoma syndrome associated with congenital orbital teratoma, caused by a PTCH1 frameshift mutationRead More
A possible chemopreventive role for photodynamic therapy in Gorlin syndrome: a report of basal cell carcinoma reduction and review of literatureRead More
Congenital linear unilateral basal cell nevus: a case report with patched gene molecular studiesRead More