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...

por 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, B
Publicado 2006

Germline mutations of the INK4a-ARF gene in patients with suspected genetic predisposition to melanoma

por Soufir, N, Lacapere, J J, Bertrand, G, Matichard, E, Meziani, R, Mirebeau, D, Descamps, V, Gérard, B, Archimbaud, A, Ollivaud, L, Bouscarat, F, Baccard, M, Lanternier, G, Saïag, P, Lebbé, C, Basset-Seguin, N, Crickx, B, Cave, H, Grandchamp, B
Publicado 2004