F. Perea

Publications69
h-index9
Citations283
Highly Influential Citations12
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Hb D-Los Angeles associated with Hb S or beta-thalassemia in four Mexican Mestizo families.
Twenty-five individuals were studied from four unrelated Mexican Mestizo families with Hb D-Los Angeles. We observed five compound heterozygotes: four for Hb S and Hb D, and one for Hb D and… Expand
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Centromere–telomere (12;8p) fusion, telomeric 12q translocation, and i(12p) trisomy 1
The concurrence of a short arm isochromosome and a translocation of the entire long arm of the same chromosome to a telomere of another chromosome, implying trisomy for 4p, 5p, 7p, 9p, 10p or 12p,… Expand
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Polymorphisms in candidate genes for type 2 diabetes mellitus in a Mexican population with metabolic syndrome findings.
The metabolic or insulin resistance syndrome, characterized by hypertension, dyslipidemia, glucose intolerance and hyperinsulinemia, may have genetic determinants. The insulin gene (INS), insulin… Expand
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β-Thalassemia and βA globin gene haplotypes in Mexican mestizos
Abstractβ-globin haplotypes of 20 β-thalassemia (β-thal) and 87 βA Mexican mestizo chromosomes were analyzed to ascertain the origin of the β-thal alleles and the frequencies and distribution of the… Expand
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HLA-DQB1, -DQA1, -DRB1 linkage disequilibrium and haplotype diversity in a Mestizo population from Guadalajara, Mexico.
HLA-DQB1, -DQA1, and -DRB1 genes were typed by polymerase chain reaction with sequence-specific primer (PCR-SSP) in 159 healthy volunteers from 32 families living in Guadalajara, Mexico. Three-locus… Expand
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Analysis of betaS and betaA genes in a Mexican population with African roots.
To investigate the origin of the beta(A) and beta(S) genes in a Mexican population with African roots and a high frequency of hemoglobin S, we analyzed 467 individuals (288 unrelated) from different… Expand
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Red cell membrane protein deficiencies in Mexican patients with hereditary spherocytosis.
Twenty-seven families and four individual patients with hereditary spherocytosis (HS) from the northwestern region of Mexico were studied. An autosomal dominant inheritance pattern was identified in… Expand
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Diversity of the 5′ β-Globin Haplotype of Four β-Thalassemia Mutations in the Mexican Population
β-Globin haplotypes have been used to investigate the origin and spread of β-globin mutations such as Hb S [β6(A3)Glu→Val, GAG>GTG], Hb E [β26(B8)Glu→Lys, GAG>AAG], and β-thalassemia (β-thal).… Expand
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Dynamics of residue decomposition in the field in a dryland rotation under Mediterranean climate conditions in southern Spain
With the aim of assessing the benefits of crop remains left on the soil surface, a study was carried out on the decomposition and characteristics of residue deposited on a clay soil in southern Spain… Expand
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Thalidomide therapy in a patient with thalassemia major.
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