Browsing by Author Ibarra, B.

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Changes in hemoglobin in patients with hemolytic anemia [Alteraciones de la hemoglobina en pacientes con anemia hemolítica.]Perez, G.; de la Pena, M.E.; Esparza, A.; Mejia, A.; Vazquez, V.; Aguilar Luna, J.C.; Gonzalez, J.; Lopez-Guido, B.; Ornelas, M.L.; Ibarra, B.--
Changes in hemoglobin in patients with hemolytic anemia [Alteraciones de la hemoglobina en pacientes con anemia hemol�tica.]Perez, G.; de la Pena, M.E.; Esparza, A.; Mejia, A.; Vazquez, V.; Aguilar Luna, J.C.; Gonzalez, J.; Lopez-Guido, B.; Ornelas, M.L.; Ibarra, B.--
Diversity of the 5? ?-globin haplotype of four ?-thalassemia mutations in the Mexican populationMorales, K.R.; Magana, M.T.; Ibarra, B.; Perea, F.J.--
Diversity of the 5′ β-globin haplotype of four β-thalassemia mutations in the Mexican populationMorales, K.R.; Magana, M.T.; Ibarra, B.; Perea, F.J.--
EGFR gene polymorphisms -216G>T and -191C>A are risk markers for gastric cancer in Mexican populationTorres-Jasso, J.H.; Marin, M.E.; Luna Santiago, E.S.; Leoner, J.C.; Torres, J.; Magana-Torres, M.T.; Perea, F.J.; Ibarra, B.; Sanchez-Lopez, J.Y.--
Electrophoretic pattern of sorbitol dehydrogenase (E.C. 1.1.1.14) in human seminal plasma and spermatozoaPerea, F.J.; Vaca, G.; Alvarez, C.; Cantu, J.M.; Ibarra, B.--
Electrophoretic pattern of sorbitol dehydrogenase (E.C. 1.1.1.14) in human seminal plasma and spermatozoaPerea, F.J.; Vaca, G.; Alvarez, C.; Cantu, J.M.; Ibarra, B.--
Fetal hemoglobin and the gamma G/gamma A chain ratio in children with acute lymphoblastic leukemia L1 and L2 [Hemoglobina fetal y relación de cadenas gamma G/gamma A en niños con leucemia aguda linfoblástica L1 y L2.]Villalobos-Arambula, A.R.; Aguilar-Luna, J.C.; Esparza, A.; Perea, F.J.; de Loza, R.; Hernandez-Cordova, A.; Ibarra, B.--
Fetal hemoglobin and the gamma G/gamma A chain ratio in children with acute lymphoblastic leukemia L1 and L2 [Hemoglobina fetal y relaci�n de cadenas gamma G/gamma A en ni�os con leucemia aguda linfobl�stica L1 y L2.]Villalobos-Arambula, A.R.; Aguilar-Luna, J.C.; Esparza, A.; Perea, F.J.; de Loza, R.; Hernandez-Cordova, A.; Ibarra, B.--
Fetal hemoglobin in children with different neoplasms [Hemoglobina fetal en niños con diferentes neoplasias.]Ibarra, B.; Montes, J.; Becerra, C.; Prea, F.J.; Barros-Nunez, P.; Aguilar-Luna, J.C.; Arroyo, J.--
Fetal hemoglobin in children with different neoplasms [Hemoglobina fetal en niños con diferentes neoplasias.]Ibarra, B.; Montes, J.; Becerra, C.; Prea, F.J.; Barros-Nunez, P.; Aguilar-Luna, J.C.; Arroyo, J.--
Genetic diversity of the IL-4, IL-4 receptor and IL-13 loci in mestizos in the general population and in patients with asthma from three subpopulations in MexicoLopez, K.I.M.; Martinez, S.E.F.; Moguel, M.C.M.; Romero, L.T.; Figueroa, C.S.; Pacheco, G.V.; Ibarra, B.; Corona, J.S.--
Genetic diversity of the IL-4, IL-4 receptor and IL-13 loci in mestizos in the general population and in patients with asthma from three subpopulations in MexicoLopez, K.I.M.; Martinez, S.E.F.; Moguel, M.C.M.; Romero, L.T.; Figueroa, C.S.; Pacheco, G.V.; Ibarra, B.; Corona, J.S.--
Genetic relationship of a Mexican Afromestizo population through the analysis of the 3′ haplotype of the β globin gene in βA chromosomesMagana, M.T.; Perea, F.J.; Gonzalez, J.R.; Ibarra, B.--
Genetic variation of the FMR1 gene among four Mexican populations: Mestizo, Huichol, Purepecha, and TarahumaraBarros-Nunez, P.; Rosales-Reynoso, M.A.; Sandoval, L.; Romero-Espinoza, P.; Troyo-Sanroman, R.; Ibarra, B.--
Genetic variation of the FMR1 gene among four Mexican populations: Mestizo, Huichol, Purepecha, and TarahumaraBarros-Nunez, P.; Rosales-Reynoso, M.A.; Sandoval, L.; Romero-Espinoza, P.; Troyo-Sanroman, R.; Ibarra, B.--
Genotoxicity produced by disease and drugsMagana, M.T.; Perea, F.J.; Gonzalez, J.R.; Ibarra, B.--
Hb D-Los Angeles associated with Hb S or ?-thalassemia in four Mexican Mestizo familiesPerea, F.J.; Casas-Castaneda, M.; Villalobos-Arambula, A.R.; Barajas, H.; Alvarez, F.; Camacho, A.; Hermosillo, R.M.; Ibarra, B.--
Hb D-Los Angeles associated with Hb S or β-thalassemia in four Mexican Mestizo familiesPerea, F.J.; Casas-Castaneda, M.; Villalobos-Arambula, A.R.; Barajas, H.; Alvarez, F.; Camacho, A.; Hermosillo, R.M.; Ibarra, B.--
HB Fannin-Lubbock-I with a single GGC>GAC mutation at ?119(GH2)Gly?Asp in a homozygous mexican patientIbarra, B.; Aizpuru, E.; Snchez-Lpez, J.Y.; Morales, K.R.; Perea, F.J.; Ruiz-Reyes, G.--