Pippucci T;Savoia A;Perrotta S;Pujol-Moix N;Noris P;Castegnaro G;Pecci A;Gnan C;Punzo F;Marconi C;Gherardi S;Loffredo G;De Rocco D;Scianguetta S;Barozzi S;Magini P;Bozzi V;Dezzani L;Di Stazio M;Ferraro M;Perini G;Seri M;Balduini CL, Mutations in the 5' UTR of ANKRD26, the ankirin repeat domain 26 gene, cause an autosomal-dominant form of inherited thrombocytopenia, THC2, «AMERICAN JOURNAL OF HUMAN GENETICS», 2011, 88, pp. 115 - 120 [Scientific article]
Wischmeijer A;Magini P;Giorda R;Gnoli M;Ciccone R;Cecconi L;Franzoni E;Mazzanti L;Romeo G;Zuffardi O;Seri M, Olfactory Receptor-Related Duplicons Mediate a Microdeletion at 11q13.2q13.4 Associated with a Syndromic Phenotype., «MOLECULAR SYNDROMOLOGY», 2011, 1, pp. 176 - 184 [Scientific article]
Pradella LM; Zuntini R; Magini P; Ceccarelli C; Neri I; Cerasoli S; Graziano C; Gasparre G; Turchetti D, Two distinct thyroid tumours in a Cowden Syndrome patient carrying both a 10q23 and a mitochondrial DNA germline deletion, «JOURNAL OF MEDICAL GENETICS», 2011, 48(11), pp. 779 - 782 [Scientific article]
Graziano C; Carone S; Panza E; Marino F; Magini P; Romeo G; Pession A; Seri M., Association of hereditary thrombocythemia and distal limb defects with a thrombopoietin gene mutation., «BLOOD», 2009, 114, pp. 1655 - 1657 [Scientific article]