Author:
Panteliadis Christos P.,Friedrich Reinhard E.
Publisher
Springer International Publishing
Reference73 articles.
1. Unden AB, Holmberg E, Lundh-Rozell B, et al. Mutations in the human homologue of drosophila patched (PTCH) in basal cell carcinomas and the Gorlin syndrome: different in vivo mechanisms of PTCH inactivation. Cancer Res. 1996;56:4562–5.
2. Fujii K, Ohashi H, Suzuki M, et al. Frameshift mutation in the PTCH2 gene can cause nevoid basal cell carcinoma syndrome. Fam Cancer. 2013;12:611–4.
3. Smith MJ, Beetz C, Williams SG, et al. Germline mutations in SUFU cause Gorlin syndrome-associated childhood medulloblastoma and redefine the risk associated with PTCH1 mutations. J Clin Oncol. 2014;32:4155–61.
4. Evans DG, Oudit D, Smith MJ, et al. First evidence of genotype-phenotype correlations in Gorlin syndrome. J Med Genet. 2017;54:530–6.
5. Jarisch W. Zur Lehre von den Hautgeschwülsten. Arch Derm Syphilol. 1894;18:162–22.