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Results: 1-12 |
Results: 12
Chromosomal abnormalities and polymorphisms in infertile men
Authors: Videau, SP Araujo, H Ballesta, F Ballesca, JL Vanrell, JA
Citation: Sp. Videau et al., Chromosomal abnormalities and polymorphisms in infertile men, ARCH ANDROL, 46(3), 2001, pp. 205-210
Systemic sarcoidosis with spleen involvement
Authors: Rodriguez-Garcia, JL Picazo, J Mira, C Ballesta, F Garcia-Nieto, JC Prieto, E
Citation: Jl. Rodriguez-garcia et al., Systemic sarcoidosis with spleen involvement, POSTG MED J, 77(906), 2001, pp. 265-265
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
SRY gene transferred to the long arm of the X chromosome in a Y-positive XX true hermaphrodite
Authors: Margarit, E Coll, MD Oliva, R Gomez, D Soler, A Ballesta, F
Citation: E. Margarit et al., SRY gene transferred to the long arm of the X chromosome in a Y-positive XX true hermaphrodite, AM J MED G, 90(1), 2000, pp. 25-28
Assaying the granulocyte-macrophage colony-stimulating factor (GM-CSP) as a mitogen of immature cells in fetal blood cultures
Authors: Costa, D Borrell, A Jou, JM Beson, I Soler, A Carrio, A Margarit, E Caballin, R Ballesta, F Fortuny, A
Citation: D. Costa et al., Assaying the granulocyte-macrophage colony-stimulating factor (GM-CSP) as a mitogen of immature cells in fetal blood cultures, PRENAT DIAG, 19(1), 1999, pp. 17-20
A presenilin 1 mutation (Ser169Pro) associated with early-onset AD and myoclonic seizures
Authors: Ezquerra, M Carnero, C Blesa, R Gelpi, JL Ballesta, F Oliva, R
Citation: M. Ezquerra et al., A presenilin 1 mutation (Ser169Pro) associated with early-onset AD and myoclonic seizures, NEUROLOGY, 52(3), 1999, pp. 566-570
alpha(1)-Antichymotrypsin gene polymorphism and susceptibility to Parkinson's disease
Authors: Munoz, E Obach, V Oliva, R Marti, MJ Ezquerra, M Pastor, P Ballesta, F Tolosa, E
Citation: E. Munoz et al., alpha(1)-Antichymotrypsin gene polymorphism and susceptibility to Parkinson's disease, NEUROLOGY, 52(2), 1999, pp. 297-301
Clinical characterization, molecular and FISH studies in 80 patients with clinical suspicion of Williams-Beuren syndrome
Authors: Mila, M Carrio, A Sanchez, A Gomez, D Jimenez, D Estivill, X Ballesta, F
Citation: M. Mila et al., Clinical characterization, molecular and FISH studies in 80 patients with clinical suspicion of Williams-Beuren syndrome, MED CLIN, 113(2), 1999, pp. 46-49
Dentatorubropallidoluysian atrophy in a Spanish family: a clinical, radiological, pathological, and genetic study
Authors: Munoz, E Mila, M Sanchez, A Latorre, P Ariza, A Codina, M Ballesta, F Tolosa, E
Citation: E. Munoz et al., Dentatorubropallidoluysian atrophy in a Spanish family: a clinical, radiological, pathological, and genetic study, J NE NE PSY, 67(6), 1999, pp. 811-814
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
Risultati: 1-12 |