Mapping of a gene for non-specific X linked mental retardation: evidence for linkage to chromosomal region Xp21.1-Xp22.3.

Por Kozák, L, Chiurazzi, P, Genuardi, M, Pomponi, M G, Zollino, M, Neri, G
Publicado em 1993

Reduced BRCA1 expression due to promoter hypermethylation in therapy-related acute myeloid leukaemia

Por Scardocci, A, Guidi, F, D'Alo', F, Gumiero, D, Fabiani, E, DiRuscio, A, Martini, M, Larocca, L M, Zollino, M, Hohaus, S, Leone, G, Voso, M T
Publicado em 2006

Cryptic telomeric rearrangements in subjects with mental retardation associated with dysmorphism and congenital malformations

Por Rossi, E., Piccini, F., Zollino, M., Neri, G., Caselli, D., Tenconi, R., Castellan, C., Carrozzo, R., Danesino, C., Zuffardi, O., Ragusa, A., Castiglia, L., Galesi, O., Greco, D., Romano, C., Pierluigi, M., Perfumo, C., Di, R, Faravelli, F., Bricarelli, F. D., Bonaglia, M., Bedeschi, M., Borgatti, R.
Publicado em 2001

Cryptic deletions are a common finding in “balanced” reciprocal and complex chromosome rearrangements: a study of 59 patients

Por De Gregori, M, Ciccone, R, Magini, P, Pramparo, T, Gimelli, S, Messa, J, Novara, F, Vetro, A, Rossi, E, Maraschio, P, Bonaglia, M C, Anichini, C, Ferrero, G B, Silengo, M, Fazzi, E, Zatterale, A, Fischetto, R, Previderé, C, Belli, S, Turci, A, Calabrese, G, Bernardi, F, Meneghelli, E, Riegel, M, Rocchi, M, SGuerneri, Lalatta, F, Zelante, L, Romano, C, Fichera, Ma, Mattina, T, Arrigo, G, Zollino, M, Giglio, S, Lonardo, F, Bonfante, A, Ferlini, A, Cifuentes, F, Van Esch, H, Backx, L, Schinzel, A, Vermeesch, J R, Zuffardi, O
Publicado em 2007