Oral manifestations in a boy with X-linked reticulate pigmentary disorder

Por Callea, M, Maglione, M, Yavuz, I, Deroma, L, Willoughby, CE, Tadini, G
Publicado em 2012

Autosomal dominant hereditary benign telangiectasia maps to the CMC1 locus for capillary malformation on chromosome 5q14

Por Brancati, F, Valente, E, Tadini, G, Caputo, V, Di, B, Gelmetti, C, Dallapiccola, B
Publicado em 2003

Phenotypic variability in a cohort of 40 Italian subjects carrying mutations in the gene EDA

Por Guazzarotti, L, Tadini, G, Mancini, GE, Giglio, S, Sani, I, Nannini, P, Bosoni, M, Bottero, A, Caimi, A, Morelli, M, Zuccotti, GV
Publicado em 2012