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:
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:
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