Microdeletion of 9q22.3: A patient with minimal deletion size associated with a severe phenotype
Click HERE to view the article on PubMed.gov. The Gorlin Syndrome Alliance [...]
A Novel Case of Gorlin Syndrome Mosaicism Involving an SMO Gene Mutation: Clinical, Histological and Molecular Analysis of Basaloid Tumours
Click HERE to view the article on PubMed.gov. The Gorlin Syndrome Alliance [...]
Novel mutation in PTCH1 gene in a patient with basal cell nevus syndrome and uterus bicornis
Click HERE to view the article on PubMed.gov. The Gorlin Syndrome Alliance [...]
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 [...]
Rhabdomyosarcoma, Wilms tumor, and deletion of the patched gene in Gorlin syndrome
Click here to view the article on PubMed. The Gorlin Syndrome Alliance [...]