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 Flex, E Capon, F Sangiuolo, F Carraro, E Gualandi, F Mazzoli, M Martini, A Novelli, G Dallapiccola, B

Citation: M. Mangino et al., Mapping of a new autosomal dominant nonsyndromic hearing loss locus (DFNA30) to chromosome 15q25-26, EUR J HUM G, 9(9), 2001, pp. 667-671

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