BHD mutations, clinical and molecular genetic investigations of Birt–Hogg–Dubé syndrome: a new series of 50 families and a review of published reports

por Toro, J R, Wei, M-H, Glenn, G M, Weinreich, M, Toure, O, Vocke, C, Turner, M, Choyke, P, Merino, M J, Pinto, P A, Steinberg, S M, Schmidt, L S, Linehan, W M
Publicado 2008