Authors:
Miano, MG
Testa, F
Filippini, F
Trujillo, M
Conte, I
Lanzara, C
Millan, JM
De Bernardo, C
Grammatico, B
Mangino, M
Torrente, I
Carrozzo, R
Simonelli, F
Rinaldi, E
Ventruto, V
D'Urso, M
Ayuso, C
Ciccodicola, A
Citation: Mg. Miano et al., Identification of novel RP2 mutations in a subset of X-linked Retinitis Pigmentosa families and prediction of new domains, HUM MUTAT, 18(2), 2001, pp. 109-119
Authors:
Mangino, M
Torrente, I
De Luca, A
Sanchez, O
Dallapiccola, B
Novelli, G
Citation: M. Mangino et al., A single-nucleotide polymorphism in the human bone morphogenetic protein-4(BMP 4) gene, J HUM GENET, 44(1), 1999, pp. 76-77
Authors:
Miano, MG
Testa, F
Strazzullo, M
Trujillo, M
De Bernardo, C
Grammatico, B
Simonelli, F
Mangino, M
Torrente, I
Ruberto, G
Beneyto, M
Antinolo, G
Rinaldi, E
Danesino, C
Ventruto, V
D'Urso, M
Ayuso, C
Baiget, M
Ciccodicola, A
Citation: Mg. Miano et al., Mutation analysis of the RPGR gene reveals novel mutations in south European patients with X-linked retinitis pigmentosa, EUR J HUM G, 7(6), 1999, pp. 687-694
Authors:
Mangino, M
Sanchez, O
Torrente, I
De Luca, A
Capon, F
Novelli, G
Dallapiccola, B
Citation: M. Mangino et al., Localization of a gene for familial patella aplasia-hypoplasia (PTLAH) to chromosome 17q21-22, AM J HU GEN, 65(2), 1999, pp. 441-447
Authors:
De Luca, A
Torrente, I
Mangino, M
Bertini, E
Dallapiccola, B
Novelli, G
Citation: A. De Luca et al., A novel mutation (R27 1X) in the myotubularin gene causes a severe miotubular myopathy, HUMAN HERED, 49(1), 1999, pp. 59-60