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Results: 1-9 |
Results: 9

Authors: Cinti, R Fava, M Sancandi, M Matera, I Ravazzolo, R Ceccherini, I
Citation: R. Cinti et al., Assignment of the HOX11L2 gene to human chromosome band 5q35.1 and of its murine homolog to mouse chromosome bands 11A4-A5 by in situ hybridization, CYTOG C GEN, 92(3-4), 2001, pp. 354-355

Authors: Mazzocco, M Arrigo, P Egeo, A Maffei, M Vergano, A Di Lisi, R Ghiotto, F Ciccone, E Cinti, R Ravazzolo, R Scartezzini, P
Citation: M. Mazzocco et al., A novel human homologue of the SH3BGR gene encodes a small protein similarto glutaredoxin 1 of Escherichia coli, BIOC BIOP R, 285(2), 2001, pp. 540-545

Authors: Lo Nigro, C Cusano, R Scaranari, M Cinti, R Forabosco, P Morra, VB De Michele, G Santoro, L Davies, S Hurst, J Devoto, M Ravazzolo, R Seri, M
Citation: C. Lo Nigro et al., A refined physical and transcriptional map of the SPG9 locus on 10q23.3-q24.2, EUR J HUM G, 8(10), 2000, pp. 777-782

Authors: Cinti, R Botta, G Asnaghi, V Del Monaco, A Salvego, M Silengo, M
Citation: R. Cinti et al., De novo partial duplication of 3q and distal deletion of 20p in a 15-week abortus with omphalocele, FETAL DIAGN, 15(1), 2000, pp. 61-62

Authors: Cinti, R Yin, L Ilc, K Berger, N Basolo, F Cuccato, S Giannini, R Torre, G Miccoli, P Amati, P Romeo, G Corvi, R
Citation: R. Cinti et al., RET rearrangements in papillary thyroid carcinomas and adenomas detected by interphase FISH, CYTOG C GEN, 88(1-2), 2000, pp. 56-61

Authors: Romio, L Musante, L Cinti, R Seri, M Moran, O Zegarra-Moran, O Galietta, LJV
Citation: L. Romio et al., Characterization of a murine gene homologous to the bovine CaCC chloride channel, GENE, 228(1-2), 1999, pp. 181-188

Authors: Puliti, A Cinti, R Betsos, N Romeo, G Ceccherini, I
Citation: A. Puliti et al., HOX11L1, a gene involved in peripheral nervous system development, maps tohuman chromosome 2p13.1 -> p12 and mouse chromosome 6C3-D1, CYTOG C GEN, 84(1-2), 1999, pp. 115-117

Authors: Seri, M Cusano, R Forabosco, P Cinti, R Caroli, F Picco, P Bini, R Morra, VB De Michele, G Lerone, M Silengo, M Pela, I Borrone, C Romeo, G Devoto, M
Citation: M. Seri et al., Genetic mapping to 10q23.3-q24.2, in a large Italian pedigree, of a new syndrome showing bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophy, AM J HU GEN, 64(2), 1999, pp. 586-593

Authors: Concolino, D Ferraro, L Cinti, R Mussari, A Strisciuglio, P
Citation: D. Concolino et al., A severe form of the tetrasomy 18p syndrome confirmed by in situ hybridization, RIV ITAL P, 24(6), 1998, pp. 1149-1152
Risultati: 1-9 |