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Results: 1-3 |
Results: 3
Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females
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
Mutation and transcription analysis of transthyretin gene in Italian families with hereditary amyloidosis: a putative novel 'hot spot' in codon 47
Authors: Ferlini, A Obici, L Manzati, E Biadi, O Tarantino, E Conigli, P Merlini, G D'Alessandro, M Mazzaferro, V Tassinari, CA Salvi, F
Citation: A. Ferlini et al., Mutation and transcription analysis of transthyretin gene in Italian families with hereditary amyloidosis: a putative novel 'hot spot' in codon 47, CLIN GENET, 57(4), 2000, pp. 284-290
Mutations in autosomal dominant polycystic kidney disease 2 gene: Reduced expression of PKD2 protein in lymphoblastoid cells
Authors: Aguiari, G Manzati, E Penolazzi, L Micheletti, F Augello, G Vitali, ED Cappelli, G Cai, YQ Reynolds, D Somlo, S Piva, R del Senno, L
Citation: G. Aguiari et al., Mutations in autosomal dominant polycystic kidney disease 2 gene: Reduced expression of PKD2 protein in lymphoblastoid cells, AM J KIDNEY, 33(5), 1999, pp. 880-885
Risultati: 1-3 |