AAAAAA

   
Results: 1-21 |
Results: 21

Authors: Kerschbaum, F Lebzelter, T Lazaro, C
Citation: F. Kerschbaum et al., Multi-colour light variation of AGB stars observed with ISO, ASTRON ASTR, 375(2), 2001, pp. 527-538

Authors: Serra, E Rosenbaum, T Nadal, M Winner, U Ars, E Estivill, X Lazaro, C
Citation: E. Serra et al., Mitotic recombination effects homozygosity for NF1 germline mutations in neurofibromas (vol 28, pg 294, 2001), NAT GENET, 29(1), 2001, pp. 100-100

Authors: Serra, E Rosenbaum, T Nadal, M Winner, U Ars, E Estivill, X Lazaro, C
Citation: E. Serra et al., Mitotic recombination effects homozygosity for NF1 germline mutations in neurofibromas, NAT GENET, 28(3), 2001, pp. 294-296

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: Lopez-Correa, C Dorschner, M Brems, H Lazaro, C Clementi, M Upadhyaya, M Dooijes, D Moog, U Kehrer-Sawatzki, H Rutkowski, JL Fryns, JP Marynen, P Stephens, K Legius, E
Citation: C. Lopez-correa et al., Recombination hotspot in NF1 microdeletion patients, HUM MOL GEN, 10(13), 2001, pp. 1387-1392

Authors: Serra, E Ars, E Ravella, A Sanchez, A Puig, S Rosenbaum, T Estivill, X Lazaro, C
Citation: E. Serra et al., Somatic NF1 mutational spectrum in benign neurofibromas: mRNA splice defects are common among point mutations, HUM GENET, 108(5), 2001, pp. 416-429

Authors: Lazaro, C Castillo, A Hernandez-Matamoros, JL Iradier, MT Garcia-Feijoo, J Benitez-del-Castillo, JM Perea, J Garcia-Sanchez, J
Citation: C. Lazaro et al., Laser in situ keratomileusis enhancement after photorefractive keratectomy, OPHTHALMOL, 108(8), 2001, pp. 1423-1429

Authors: Lazaro, C Arevalo, MJ Claret, A Rodriguez, E Olivares, I
Citation: C. Lazaro et al., uvby beta photometry of the short-period binary VV Ursae Majoris, M NOT R AST, 325(2), 2001, pp. 617-630

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: Serra, E Rosenbaum, T Winner, U Aledo, R Ars, E Estivill, X Lenard, HG Lazaro, C
Citation: E. Serra et al., Schwann cells harbor the somatic NF1 mutation in neurofibromas: evidence of two different Schwann cell subpopulations, HUM MOL GEN, 9(20), 2000, pp. 3055-3064

Authors: Ars, E Serra, E Garcia, J Kruyer, H Gaona, A Lazaro, C Estivill, X
Citation: E. Ars et al., Mutations affecting mRNA splicing are the most common molecular defects inpatients with neurofibromatosis type 1, HUM MOL GEN, 9(2), 2000, pp. 237-247

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: Ars, E Serra, E de la Luna, S Estivill, X Lazaro, C
Citation: E. Ars et al., Cold shock induces the insertion of a cryptic exon in the neurofibromatosis type 1 (NF1) mRNA, NUCL ACID R, 28(6), 2000, pp. 1307-1312

Authors: Correa, CL Brems, H Lazaro, C Marynen, P Legius, E
Citation: Cl. Correa et al., Unequal meiotic crossover: A frequent cause of NF1 microdeletions, AM J HU GEN, 66(6), 2000, pp. 1969-1974

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: Correa, CL Brems, H Lazaro, C Estivill, X Clementi, M Mason, S Rutkowski, JL Marynen, P Legius, E
Citation: Cl. Correa et al., Molecular studies in 20 submicroscopic neurofibromatosis type 1 gene deletions, HUM MUTAT, 14(5), 1999, pp. 387-393

Authors: Ars, E Kruyer, H Gaona, A Serra, E Lazaro, C Estivill, X
Citation: E. Ars et al., Prenatal diagnosis of sporadic neurofibromatosis type 1 (NF1) by RNA and DNA analysis of a splicing mutation, PRENAT DIAG, 19(8), 1999, pp. 739-742

Authors: Ruiz, A Puig, S Malvehy, J Lazaro, C Lynch, M Gimenez-Arnau, AM Puig, L Sanchez-Conejo, J Estivill, X Tel, TC
Citation: A. Ruiz et al., CDKN2A mutations in Spanish cutaneous malignant melanoma families and patients with multiple melanomas and other neoplasia, J MED GENET, 36(6), 1999, pp. 490-493

Authors: Arevalo, MJ Lazaro, C
Citation: Mj. Arevalo et C. Lazaro, Time-resolved spectroscopy of RS Canum Venaticorum short-period systems. II. RT Andromedae, WY Cancri, and XY Ursae Majoris, ASTRONOM J, 118(2), 1999, pp. 1015-1033
Risultati: 1-21 |