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