Nevoid basal carcinoma syndrome (Gorlin syndrome) and pronounced androgenic alopecia in a woman with a novel mutation p.Leu1159fsx32 in the PTCH gene
Sofia KITSIOU-TZELI, Patrick WILLEMS, Maria KOSMADAKI, Eleni LEZE, Christine VRETTOU, Emmanuel KANAVAKIS, Alexandra KATSAROUVolume:
38
Year:
2011
Language:
english
Pages:
4
DOI:
10.1111/j.1346-8138.2011.01265.x
File:
PDF, 290 KB
english, 2011