Browsing by Author Perea, F.J.

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3? haplotypes of the ?-globin gene in ? s- chromosomes of Mexican individualsMagana, M.T.; Perea, F.J.; Ongay, Z.; Ibarra, B.--
3′ haplotypes of the β-globin gene in β s- chromosomes of Mexican individualsMagana, M.T.; Perea, F.J.; Ongay, Z.; Ibarra, B.--
A frameshift at codons 77/78 (-C): A novel ?-thalassemia mutationPerea, F.J.; Magana, M.T.; Esparza, M.A.; Ibarra, B.--
A frameshift at codons 77/78 (-C): A novel β-thalassemia mutationPerea, F.J.; Magana, M.T.; Esparza, M.A.; Ibarra, B.--
?A globin gene haplotypes in mexican huichols: genetic relatedness to other populationsVillalobos-Arambula, A.R.; Rivas, F.; Sandoval, L.; Perea, F.J.; Casas-Castaneda, M.; Cantu, J.M.; Ibarra, B.--
Alpha-thalassemia in a selected population of MexicoCasas-Castaneda, M.; Hernandez-Lugo, I.; Torres, O.; Barajas, H.; Cibrian, S.; Zamudio, G.; Villalobos-Arambula, A.R.; Hermosillo-Banuelos, R.M.; Perea, F.J.; Ibarra, B.--
Alpha-thalassemia in a selected population of MexicoCasas-Castaneda, M.; Hernandez-Lugo, I.; Torres, O.; Barajas, H.; Cibrian, S.; Zamudio, G.; Villalobos-Arambula, A.R.; Hermosillo-Banuelos, R.M.; Perea, F.J.; Ibarra, B.--
Analysis of the SLC4A1 gene in three Mexican patients with hereditary spherocytosis: Report of a novel mutationSanchez-Lopez, J.Y.; Camacho-Torres, A.L.; Ibarra, B.; Tintos, J.A.; Perea, F.J.--
Analysis of the SLC4A1 gene in three Mexican patients with hereditary spherocytosis: Report of a novel mutationSanchez-Lopez, J.Y.; Camacho-Torres, A.L.; Ibarra, B.; Tintos, J.A.; Perea, F.J.--
Characterization of the 5? and 3? breakpoints of the Spanish (??)0-thalassemia deletion in Mexican patientsGuzman, L.F.; Perea, F.J.; Morales-Gonzalez, K.R.; Sanchez-Lopez, J.Y.; De La Cruz, E.I.; Chavez-Velasco, M.L.; Ibarra, C.B.--
Characterization of the 5′ and 3′ breakpoints of the Spanish (δβ)0-thalassemia deletion in Mexican patientsGuzman, L.F.; Perea, F.J.; Morales-Gonzalez, K.R.; Sanchez-Lopez, J.Y.; De La Cruz, E.I.; Chavez-Velasco, M.L.; Ibarra, C.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.--
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.--
Genotoxicity produced by disease and drugsMagana, M.T.; Perea, F.J.; Gonzalez, J.R.; Ibarra, B.--