Authors: Galluzzi, G Deidda, G Cacurri, S Colantoni, L Piazzo, N Vigneti, E Ricci, E Servidei, S Merico, B Pachi, A Brambati, B Mangiola, F Tonali, P Felicetti, L

Citation: G. Galluzzi et al., Molecular analysis of 4q35 rearrangements in facioscapulohumeral muscular dystrophy (FSHD): application to family studies for a correct genetic advice and a reliable prenatal diagnosis of the disease, NEUROMUSC D, 9(3), 1999, pp. 190-198

Authors: Ricci, E Galluzzi, G Deidda, G Cacurri, S Colantoni, L Merico, B Piazzo, N Servidei, S Vigneti, E Pasceri, V Silvestri, G Mirabella, M Mangiola, F Tonali, P Felicetti, L

Citation: E. Ricci et al., Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical phenotype, ANN NEUROL, 45(6), 1999, pp. 751-757