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Results:
1-11
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Results: 11
Authors:
Lopez-Bigas, N
Olive, M
Rabionet, R
Ben-David, O
Martinez-Matos, JA
Bravo, O
Banchs, I
Volpini, V
Gasparini, P
Avraham, KB
Ferrer, I
Arbones, ML
Estivill, X
Citation: N. Lopez-bigas et al., Connexin 31 (GJB3) is expressed in the peripheral and auditory nerves and causes neuropathy and hearing impairment, HUM MOL GEN, 10(9), 2001, pp. 947-952
Authors:
Badenas, C
Castellvi-Bel, S
Volpini, V
Jimenez, D
Sanchez, A
Estivill, X
Mila, M
Citation: C. Badenas et al., Linkage analysis in Spanish families with nonspecific X-linked mental retardation: Significant linkage at Xq13-q21, AM J MED G, 98(4), 2001, pp. 343-347
Authors:
Fillat, C
Espanol, T
Oset, M
Ferrando, M
Estivill, X
Volpini, V
Citation: C. Fillat et al., Identification of WASP mutations in 14 Spanish families with Wiskott-Aldrich syndrome, AM J MED G, 100(2), 2001, pp. 116-121
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:
Gaspar, C
Lopes-Cendes, I
Hayes, S
Goto, J
Arvidsson, K
Dias, A
Silveira, I
Maciel, P
Coutinho, P
Lima, M
Zhou, YX
Soong, BW
Watanabe, M
Giunti, P
Stevanin, G
Riess, O
Sasaki, H
Hsieh, M
Nicholson, GA
Brunt, E
Higgins, JJ
Lauritzen, M
Tranebjaerg, L
Volpini, V
Wood, N
Ranum, L
Tsuji, S
Brice, A
Sequeiros, J
Rouleau, GA
Citation: C. Gaspar et al., Ancestral origins of the Machado-Joseph disease mutation: A worldwide haplotype study, AM J HU GEN, 68(2), 2001, pp. 523-528
Authors:
Combarros, O
Infante, J
Lopez-Hoyos, M
Bartolome, MJ
Berciano, J
Corral, J
Volpini, V
Citation: O. Combarros et al., Celiac disease and idiopathic cerebellar ataxia, NEUROLOGY, 54(12), 2000, pp. 2346-2346
Authors:
Pujana, MA
Corral, J
Gratacos, M
Combarros, O
Berciano, J
Genis, D
Banchs, I
Estivill, X
Volpini, V
Citation: Ma. Pujana et al., Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases (vol 104, pg 516, 1999), HUM GENET, 105(4), 1999, pp. 376-376
Authors:
Pujana, MA
Corral, J
Gratacos, M
Combarros, O
Berciano, J
Genis, D
Banchs, I
Estivill, X
Volpini, V
Citation: Ma. Pujana et al., Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases, HUM GENET, 104(6), 1999, pp. 516-522
Authors:
Martorell, L
Pujana, MA
Valero, J
Joven, J
Volpini, V
Labad, A
Estivill, X
Vilella, E
Citation: L. Martorell et al., Anticipation is not associated with CAG repeat expansion in parent-offspring pairs of patients affected with schizophrenia, AM J MED G, 88(1), 1999, pp. 50-56
Authors:
Sanchez, B
Robledo, M
Biarnes, J
Saez, ME
Volpini, V
Benitez, J
Navarro, E
Ruiz, A
Antinolo, G
Borrego, S
Citation: B. Sanchez et al., High prevalence of the C634Y mutation in the RET proto-oncogene in MEN 2A families in Spain, J MED GENET, 36(1), 1999, pp. 68-70
Authors:
Gomez, JM
Biarnes, J
Volpini, V
Marti, T
Citation: Jm. Gomez et al., Neuromas and prominent corneal nerves without MEN 2B, ANN ENDOCR, 59(6), 1998, pp. 492-494
Risultati:
1-11
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