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Hemoglobin|February 12, 2009
Diversity of the 5' beta-globin haplotype of four beta-thalassemia mutations in the Mexican populationKarina R Morales, Maria T Magaña, Bertha Ibarra, et al.
Hemoglobin|October 16, 2004
A frameshift at codons 77/78 (-C): a novel beta-thalassemia mutationFrancisco J Perea, M Teresa Magaña, M Amparo Esparza, et al.
Genetics and Molecular Biology|June 4, 2011
Analysis of the SLC4A1 gene in three Mexican patients with hereditary spherocytosis: Report of a novel mutationJosefina Y Sánchez-López, Ana L Camacho-Torres, Bertha Ibarra, et al.
Hemoglobin|December 5, 2009
HB Fannin-Lubbock-I with a single GGC>GAC mutation at beta119(GH2)Gly-->Asp in a homozygous Mexican patientBertha Ibarra, Edna Aizpuru, J Yoaly Sánchez-López, et al.
Hemoglobin|November 17, 2010
Hb S [β6(A3)Glu→Val, GAG>GTG] in Mexican Mestizos: frequency and analysis of the 5' β-globin haplotypeLuis F Guzmán, Francisco J Perea, María T Magaña, et al.
Hemoglobin|August 10, 2017
A Novel 31.1 kb α-Thalassemia Deletion (- -MEX3) Found in a Mexican FamilyVíctor M Rentería-López, Francisco J Perea-Díaz, Lourdes C Rizo-delaTorre, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|December 4, 2020
Autosomal dominant early onset Alzheimer's disease in the Mexican state of Jalisco: High frequency of the mutation PSEN1 c.1292C>A and phenotypic profile of patientsSofia Dumois-Petersen, Martha P Gallegos-Arreola, María T Magaña-Torres, et al.
Hemoglobin|January 22, 2011
Characterization of the 5' and 3' breakpoints of the Spanish (δβ)0-thalassemia deletion in Mexican patientsLuis F Guzmán, Francisco J Perea, Karina R Morales-González, et al.
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