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Results:
1-8
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Results: 8
Authors:
de Cid, R
Chomel, JC
Lazaro, C
Sunyer, J
Baudis, M
Casals, T
Le Moual, N
Kitzis, A
Feingold, J
Anto, J
Estivill, X
Kauffmann, F
Citation: R. De Cid et al., CFTR and asthma in the French EGEA study, EUR J HUM G, 9(1), 2001, pp. 67-69
Authors:
de Cid, R
Volpini, V
Almasy, L
Otero, D
Estivill, X
Lazaro, C
Citation: R. De Cid et al., Analysis of the susceptibility regions to psoriasis in Spanish population:evidence of a major gene involved in psoriasis in 6p21, MED CLIN, 117(2), 2001, pp. 49-51
Authors:
Laitinen, T
Ollikainen, V
Lazaro, C
Kauppi, P
de Cid, R
Anto, JM
Estivill, X
Lokki, H
Mannila, H
Laitinen, LA
Kere, J
Citation: T. Laitinen et al., Association study of the chromosomal region containing the FCER2 gene suggests it has a regulatory role in atopic disorders, AM J R CRIT, 161(3), 2000, pp. 700-706
Authors:
Soriano, JB
de Cid, R
Estivill, X
Anto, JM
Sunyer, J
Otero, D
Roca, J
Rodriguez-Roisin, R
Morell, F
Rodrigo, MJ
Ercilla, G
Beaty, TH
Lazaro, C
Citation: Jb. Soriano et al., Association study of proposed candidate genes/regions in a population of Spanish asthmatics, EUR J EPID, 16(8), 2000, pp. 745-750
Authors:
Bombieri, C
Giorgi, S
Carles, S
de Cid, R
Belpinati, F
Tandoi, C
Pallares-Ruiz, N
Lazaro, C
Ciminelli, BM
Romey, MC
Casals, T
Pompei, F
Gandini, G
Claustres, M
Estivill, X
Pignatti, PF
Modiano, G
Citation: C. Bombieri et al., A new approach for identifying non-pathogenic mutations. An analysis of the cystic fibrosis transmembrane regulator gene in normal individuals, HUM GENET, 106(2), 2000, pp. 172-178
Authors:
Torrents, D
Mykkanen, J
Pineda, M
Feliubadalo, L
Estevez, R
de Cid, R
Sanjurjo, P
Zorzano, A
Nunes, V
Huoponen, K
Reinikainen, A
Simell, O
Savontaus, ML
Aula, P
Palacin, M
Citation: D. Torrents et al., Identification of SLC7A7, encoding y(+)LAT-1, as the lysinuric protein intolerance gene, NAT GENET, 21(3), 1999, pp. 293-296
Authors:
Lazaro, C
de Cid, R
Sunyer, J
Soriano, J
Gimenez, J
Alvarez, M
Casals, T
Anto, JM
Estivill, X
Citation: C. Lazaro et al., Missense mutations in the cystic fibrosis gene in adult patients with asthma, HUM MUTAT, 14(6), 1999, pp. 510-519
Authors:
Lopez-Bigas, N
Rabionet, R
de Cid, R
Govea, N
Gasparini, P
Zelante, L
Arbones, ML
Estivill, X
Citation: N. Lopez-bigas et al., Splice-site mutation in the PDS gene may result in intrafamilial variability for deafness in Pendred syndrome, HUM MUTAT, 14(6), 1999, pp. 520-526
Risultati:
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