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Results: 1-5 |
Results: 5

Authors: Armstrong, J Poo, P Pineda, M Aibar, E Gean, E Catala, V Monros, E
Citation: J. Armstrong et al., Classic Rett syndrome in a boy as a result of somatic mosaicism for a MECP2 mutation, ANN NEUROL, 50(5), 2001, pp. 692-692

Authors: Armstrong, J Pineda, M Monros, E
Citation: J. Armstrong et al., Mutation analysis of 16S rRNA in patients with Rett syndrome, PED NEUROL, 23(1), 2000, pp. 85-87

Authors: Cardo, E Monros, E Colome, C Artuch, R Campistol, J Pineda, M Vilaseca, MA
Citation: E. Cardo et al., Children with stroke: Polymorphism of the MTHFR gene, mild hyperhomocysteinemia, and vitamin status, J CHILD NEU, 15(5), 2000, pp. 295-298

Authors: Canizares, J Blanca, JM Navarro, JA Monros, E Palau, F Molto, MD
Citation: J. Canizares et al., dfh is a Drosophila homolog of the Friedreich's ataxia disease gene, GENE, 256(1-2), 2000, pp. 35-42

Authors: De Castro, M Garcia-Planells, J Monros, E Canizares, J Vazquez-Manrique, R Vilchez, JJ Urtasun, M Lucas, M Navarro, G Izquierdo, G Molto, MD Palau, F
Citation: M. De Castro et al., Genotype and phenotype analysis of Friedreich's ataxia compound heterozygous patients, HUM GENET, 106(1), 2000, pp. 86-92
Risultati: 1-5 |