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:
David, A
Bitoun, P
Lacombe, D
Lambert, JC
Nivelon, A
Vigneron, J
Verloes, A
Citation: A. David et al., Hydrometrocolpos and polydactyly: a common neonatal presentation of Bardet-Biedl and McKusick-Kaufman syndromes, J MED GENET, 36(8), 1999, pp. 599-603