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Results: 1-6 |
Results: 6

Authors: De Grandi, A Calvari, V Bertini, V Bulfone, A Peverali, G Camerino, G Borsani, G Guioli, S
Citation: A. De Grandi et al., The expression pattern of a mouse doublsex-related gene is consistent witha role in gonadal differentiation, MECH DEVEL, 90(2), 2000, pp. 323-326

Authors: Calvari, V Bertini, V De Grandi, A Peverali, G Zuffardi, O Ferguson-Smith, M Knudtzon, J Camerino, G Borsani, G Guioli, S
Citation: V. Calvari et al., A new submicroscopic deletion that refines the 9p region for sex reversal, GENOMICS, 65(3), 2000, pp. 203-212

Authors: Feliubadalo, L Font, M Purroy, J Rousaud, F Estivill, X Nunes, V Golomb, E Centola, M Aksentijevich, I Kreiss, Y Goldman, B Pras, M Kastner, DL Pras, E Gasparini, P Bisceglia, L Beccia, E Gallucci, M de Sanctis, L Ponzone, A Rizzoni, GF Zelante, L Bassi, MT George, AL Manzoni, M De Grandi, A Riboni, M Endsley, JK Ballabio, A Borsani, G Reig, N Fernandez, E Estevez, R Pineda, M Torrents, D Camps, M Lloberas, J Zorzano, A Palacin, M
Citation: L. Feliubadalo et al., Non-type I cystinuria caused by mutations in SLC7A9, encoding a subunit (b(o,+)AT) of rBAT, NAT GENET, 23(1), 1999, pp. 52-57

Authors: Borsani, G Bassi, MT Sperandeo, MP De Grandi, A Buoninconti, A Riboni, M Manzoni, M Incerti, B Pepe, A Andria, G Ballabio, A Sebastio, G
Citation: G. Borsani et al., SLC7A7, encoding a putative permease-related protein, is mutated in patients with lysinuric protein intolerance, NAT GENET, 21(3), 1999, pp. 297-301

Authors: Bassi, MT Sperandeo, MP Incerti, B Bulfone, A Pepe, A Surace, EM Gattuso, C De Grandi, A Buoninconti, A Riboni, M Manzoni, M Andria, G Ballabio, A Borsani, G Sebastio, G
Citation: Mt. Bassi et al., SLC7A8, a gene mapping within the lysinuric protein intolerance critical region, encodes a new member of the glycoprotein-associated amino acid transporter family, GENOMICS, 62(2), 1999, pp. 297-303

Authors: Bassi, MT Ramesar, RS Caciotti, B Winship, IM De Grandi, A Riboni, M Townes, PL Beighton, P Ballabio, A Borsani, G
Citation: Mt. Bassi et al., X-linked late-onset sensorineural deafness caused by a deletion involving OA1 and a novel gene containing WD-40 repeats, AM J HU GEN, 64(6), 1999, pp. 1604-1616
Risultati: 1-6 |