Francisco J. Diaz-Perea
Guadalajara, JAL, Mexico
Last Updated: 09/26/2026
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Found 14 publications
Genetic Analysis of 23 SNVs of Nine Genes Involved in RBC Membranopathies with the Hematological Parameters of Mexican Patients.
Journal: Genetic testing and molecular biomarkers
Published: February 03, 2026
Mexican Patients With Suspected 22q11.2 Deletion Syndrome: Clinical Characterization and Molecular Findings by Fluorescence In Situ Hybridization and Multiplex Ligation-Dependent Probe Amplification.
Journal: Molecular genetics & genomic medicine
Published: May 19, 2025
Single nucleotide polymorphism rs4961 in the adducin 1 gene is not associated with gastric cancer or preneoplastic cancer lesions.
Journal: Oncology letters
Published: January 19, 2024
Frequency of rs1051338 and rs116928232 Variants in Individuals from Northwest Mexico.
Journal: Journal of clinical laboratory analysis
Published: January 10, 2024
Fetal hemoglobin regulating genetic variants identified in homozygous (HbSS) and heterozygous (HbSA) subjects from South Mexico.
Journal: Journal of tropical pediatrics
Published: September 21, 2022
Effects of SPTA1 Gene Variants on the Hematological Phenotype of Mexican Patients with Hereditary Spherocytosis.
Journal: Genetic testing and molecular biomarkers
Published: May 31, 2022
Hematological and molecular analysis of patients with G6PD deficiency revealed coexistent hereditary spherocytosis and alpha thalassemia.
Journal: Annals of human genetics
Published: July 13, 2021
Molecular and Hematological Analysis of Alpha- and Beta-Thalassemia in a Cohort of Mexican Patients.
Molecular and Hematological Analysis of Alpha- and Beta-Thalassemia in a Cohort of Mexican Patients.
Journal: Genetic testing and molecular biomarkers
Published: March 18, 2021
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 patients.
Journal: American journal of medical genetics. Part C, Seminars in medical genetics
Published: September 10, 2020
A Novel 31.1 kb α-Thalassemia Deletion (- -MEX3) Found in a Mexican Family.
Journal: Hemoglobin
Published: August 10, 2017
Association of polymorphisms of the TNFRSF11B and TNFSF11 genes with bone mineral density in postmenopausal women from western Mexico.
Journal: Archives of medical science : AMS
Published: March 09, 2017
Last Updated: 09/26/2026