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Results: 1-8 |
Results: 8
Detection of the presenilin 1 gene mutation (M139T) in early-onset familial Alzheimer disease in Spain
Authors: Queralt, R Ezquerra, M Castellvi, M Lleo, A Blesa, R Oliva, R
Citation: R. Queralt et al., Detection of the presenilin 1 gene mutation (M139T) in early-onset familial Alzheimer disease in Spain, NEUROSCI L, 299(3), 2001, pp. 239-241
A growth cycle characterisation and forecasting of the Spanish economy: 1970-1998
Authors: Garcia-Ferrer, A Queralt, R Blazquez, C
Citation: A. Garcia-ferrer et al., A growth cycle characterisation and forecasting of the Spanish economy: 1970-1998, INT J FOREC, 17(3), 2001, pp. 517-532
A novel presenilin 2 gene mutation (D439A) in a patient with early-onset Alzheimer's disease
Authors: Lleo, A Blesa, R Gendre, J Castellvi, M Pastor, P Queralt, R Oliva, R
Citation: A. Lleo et al., A novel presenilin 2 gene mutation (D439A) in a patient with early-onset Alzheimer's disease, NEUROLOGY, 57(10), 2001, pp. 1926-1928
Analysis of the polymorphic (GT)(n) repeat at the dopamine beta-hydroxylase gene in Spanish patients affected by schizophrenia
Authors: Arrufat, FJ Diaz, R Queralt, R Navarro, V Marcos, T Massana, G Massana, J Ballesta, F Oliva, R
Citation: Fj. Arrufat et al., Analysis of the polymorphic (GT)(n) repeat at the dopamine beta-hydroxylase gene in Spanish patients affected by schizophrenia, AM J MED G, 96(1), 2000, pp. 88-92
Paternal isodisomy 13 in a normal newborn infant after trisomy rescue evidenced by prenatal diagnosis
Authors: Soler, A Margarit, E Queralt, R Carrio, A Costa, D Gomez, D Ballesta, F
Citation: A. Soler et al., Paternal isodisomy 13 in a normal newborn infant after trisomy rescue evidenced by prenatal diagnosis, AM J MED G, 90(4), 2000, pp. 291-293
Trisomy/tetrasomy 21 mosaicism in CVS: interpretation of cytogenetic discrepancies between placental and fetal chromosome complements
Authors: Soler, A Margarit, E Carrio, A Costa, D Queralt, R Ballesta, F
Citation: A. Soler et al., Trisomy/tetrasomy 21 mosaicism in CVS: interpretation of cytogenetic discrepancies between placental and fetal chromosome complements, J MED GENET, 36(4), 1999, pp. 333-334
Parental origin and meiotic stage of non-disjunction in 139 cases of trisomy 21
Authors: Ballesta, F Queralt, R Gomez, D Solsona, E Guitart, M Ezquerra, M Moreno, J Oliva, R
Citation: F. Ballesta et al., Parental origin and meiotic stage of non-disjunction in 139 cases of trisomy 21, ANN GENET, 42(1), 1999, pp. 11-15
Cloning, sequencing and characterization of the rat hereditary hemochromatosis promoter: comparison of the human, mouse and rat HFE promoter regions
Authors: Sanchez, M Queralt, R Bruguera, M Rodes, J Oliva, R
Citation: M. Sanchez et al., Cloning, sequencing and characterization of the rat hereditary hemochromatosis promoter: comparison of the human, mouse and rat HFE promoter regions, GENE, 225(1-2), 1998, pp. 77-87
Risultati: 1-8 |