![](/img/cover-not-exists.png)
PTCH mutations and deletions in patients with typical nevoid basal cell carcinoma syndrome and in patients with a suspected genetic predisposition to basal cell carcinoma: a French study
Soufir, N, Gerard, B, Portela, M, Brice, A, Liboutet, M, Saiag, P, Descamps, V, Kerob, D, Wolkenstein, P, Gorin, I, Lebbe, C, Dupin, N, Crickx, B, Basset-Seguin, N, Grandchamp, BVolume:
95
Language:
english
Journal:
British Journal of Cancer
DOI:
10.1038/sj.bjc.6603303
Date:
August, 2006
File:
PDF, 96 KB
english, 2006