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Results: 1-6 |
Results: 6

Authors: Crisponi, L Deiana, M Loi, A Chiappe, F Uda, M Amati, P Bisceglia, L Zelante, L Nagaraja, R Porcu, S Ristaldi, MS Marzella, R Rocchi, M Nicolino, M Lienhardt-Roussie, A Nivelon, A Verloes, A Schlessinger, D Gasparini, P Bonneau, D Cao, A Pilia, G
Citation: L. Crisponi et al., The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome, NAT GENET, 27(2), 2001, pp. 159-166

Authors: Taillon-Miller, P Bauer-Sardina, I Saccone, NL Putzel, J Laitinen, T Cao, A Kere, J Pilia, G Rice, JP Kwok, PY
Citation: P. Taillon-miller et al., Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28, NAT GENET, 25(3), 2000, pp. 324-328

Authors: Pilia, G Uda, M Macis, D Frau, F Crisponi, L Balli, F Barbera, C Colombo, C Frediani, T Gatti, R Iorio, R Marazzi, MG Marcellini, M Musumeci, S Nebbia, G Vajro, P Ruffa, G Zancan, L Cao, A DeVirgilis, S
Citation: G. Pilia et al., Jagged-1 mutation analysis in Italian Alagille syndrome patients, HUM MUTAT, 14(5), 1999, pp. 394-400

Authors: Huber, R Hansen, RS Strazzullo, M Pengue, G Mazzarella, R D'Urso, M Schlessinger, D Pilia, G Gartler, SM D'Esposito, M
Citation: R. Huber et al., DNA methylation in transcriptional repression of two differentially expressed X-linked genes, GPC3 and SYBL1, P NAS US, 96(2), 1999, pp. 616-621

Authors: Pellegrini, M Pilia, G Pantano, S Lucchini, F Uda, M Fumi, M Cao, A Schlessinger, D Forabosco, A
Citation: M. Pellegrini et al., Gpc3 expression correlates with the phenotype of the Simpson-Golabi-Behmelsyndrome, DEV DYNAM, 213(4), 1998, pp. 431-439

Authors: Huber, R Mazzarella, R Chen, CN Chen, E Ireland, M Lindsay, S Pilia, G Crisponi, L
Citation: R. Huber et al., Glypican 3 and glypican 4 are juxtaposed in Xq26.1, GENE, 225(1-2), 1998, pp. 9-16
Risultati: 1-6 |