Authors:
Claustres, M
Guittard, C
Bozon, D
Chevalier, F
Verlingue, C
Ferec, C
Girodon, E
Cazeneuve, C
Bienvenu, T
Lalau, G
Dumur, V
Feldmann, D
Bieth, E
Blayau, M
Clavel, C
Creveaux, I
Malinge, MC
Monnier, N
Malzac, P
Mittre, H
Chomel, JC
Bonnefont, JP
Iron, A
Chery, M
Des Georges, M
Citation: M. Claustres et al., Spectrum of CFTR mutations in cystic fibrosis and in congenital absence ofthe vas deferens in France, HUM MUTAT, 16(2), 2000, pp. 143-156
Authors:
Davril, M
Degroote, S
Humbert, P
Galabert, C
Dumur, V
Lafitte, JJ
Lamblin, G
Roussel, P
Citation: M. Davril et al., The sialylation of bronchial mucins secreted by patients suffering from cystic fibrosis or from chronic bronchitis is related to the severity of airway infection, GLYCOBIOLOG, 9(3), 1999, pp. 311-321
Authors:
Des Georges, M
Guittard, C
Bozon, D
Chevalier, F
Verlingue, C
Ferec, C
Girodon, E
Cazeneuve, C
Bienvenu, T
Lalau, G
Dumur, V
Feldmann, D
Bieth, E
Blayau, M
Clavel, C
Creveaux, I
Malinge, MC
Monnier, N
Malzac, P
Mittre, H
Bonnefont, JP
Iron, A
Chomel, JC
Chery, M
Claustres, M
Citation: M. Des Georges et al., Molecular basis of cystic fibrosis in France: more than 300 different mutations and 506 genotypes are involved, M S-MED SCI, 14(12), 1998, pp. 1413-1421