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Results: 1-6 |
Results: 6

Authors: Vacca, M Filippini, F Budillon, A Rossi, V Mercadante, G Manzati, E Gualandi, F Bigoni, S Trabanelli, C Pini, G Calzolari, E Ferlini, A Meloni, I Hayek, G Zappella, M Renieri, A D'Urso, M D'Esposito, M MacDonald, F Kerr, A Dhanjal, S Hulten, M
Citation: M. Vacca et al., Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females, J MOL MED-J, 78(11), 2001, pp. 648

Authors: Zappella, M Meloni, I Longo, I Hayek, G Renieri, A
Citation: M. Zappella et al., Preserved speech variants of the Rett syndrome: Molecular and clinical analysis, AM J MED G, 104(1), 2001, pp. 14-22

Authors: De Bona, C Zappella, M Hayek, G Meloni, I Vitelli, F Bruttini, M Cusano, R Loffredo, P Longo, I Renieri, A
Citation: C. De Bona et al., Preserved speech variant is allelic of classic Rett syndrome, EUR J HUM G, 8(5), 2000, pp. 325-330

Authors: Vitelli, F Meloni, I Fineschi, S Favara, F Storlazzi, CT Rocchi, M Renieri, A
Citation: F. Vitelli et al., Identification and characterization of mouse orthologs of the AMMECR1 and FACL4 genes deleted in AMME syndrome: orthology of Xq22.3 and MmuXF1-F3, CYTOG C GEN, 88(3-4), 2000, pp. 259-263

Authors: Bruttini, M Vitelli, F Meloni, I Rizzari, C Della Volpe, M Mazzucco, G De Marchi, M Renieri, A
Citation: M. Bruttini et al., Mosaicism in Alport syndrome and genetic counselling, J MED GENET, 37(9), 2000, pp. 717-719

Authors: Meloni, I Bruttini, M Longo, I Mari, F Rizzolio, F D'Adamo, P Denvriendt, K Fryns, JP Toniolo, D Renieri, A
Citation: I. Meloni et al., A mutation in the Rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in males, AM J HU GEN, 67(4), 2000, pp. 982-985
Risultati: 1-6 |