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Familial Cancer|March 25, 2014
Intronic splicing mutations in PTCH1 cause Gorlin syndromeZaynab Bholah, Miriam J Smith, Helen J Byers, et al.European Journal of Human Genetics : EJHG|August 28, 2014
Common variants modify the age of onset for basal cell carcinomas in Gorlin syndromeBinnaz Yasar, Helen J Byers, Miriam J Smith, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|November 19, 2014
Germline mutations in SUFU cause Gorlin syndrome-associated childhood medulloblastoma and redefine the risk associated with PTCH1 mutationsMiriam J Smith, Christian Beetz, Simon G Williams, et al.Pageof 1