Add to ORKGWe have detected, for the first time in Spain, a beta degrees thalassemia caused by the mutation IVS II-1 (G-->A). This mutation, relatively frequent in Mediterranean countries, is very rare in the Iberian peninsula. This finding besides its epidemiological relevance, increases knowledge of the spectrum of Spanish mutations of beta thalassemia
?-Thalassemia (?-thal) is present in 59% and 75% of patients with abnormal hemoglobin disorders in n...
The preliminary results of a pilot study are reported, intended as an initiation of a research plan,...
<div><p>ABSTRACT Introduction: Beta-thalassemia is caused by a deficient synthesis of the ß-chain o...
Background: Analyses of the genomic variation in the western Mediterranean population are being used...
We characterized the genetic nature of beta-thalassaemia in northern Portugal. Of the 164 patients s...
The molecular basis of beta-thalassemia was investigated at the DNA level in 28 Belgians from 14 unr...
In this study, we sought to clarity the molecular basis of a dominant inherited beta-thalassemia, fo...
Mediterranean regions the most common b-tha-lassemia mutations are due to point mutations in gene re...
In this study we have carried out alpha- and beta-globin gene analysis and defined the beta-globin g...
Beta-thalassaemia, a widespread autosomal recessive disorder, occurs sporadically in Northern and We...
In this study we have carried out haplotype analysis at the beta-globin gene cluster and defined the...
Here we describe the identification of the rare -thalassemia mutation IVS-I-130 (G-
The main hereditary hemoglobin (Hb) disorder in Argentina is b-thalassemia (b-thal). Molecular studi...
The various clinical phenotypes in beta-thalassemias have stimulated the study of genetic factors th...
Thalassemia is a Mendelian inherited blood disease caused by alpha- and beta-globin gene mutations, ...
?-Thalassemia (?-thal) is present in 59% and 75% of patients with abnormal hemoglobin disorders in n...
The preliminary results of a pilot study are reported, intended as an initiation of a research plan,...
<div><p>ABSTRACT Introduction: Beta-thalassemia is caused by a deficient synthesis of the ß-chain o...
Background: Analyses of the genomic variation in the western Mediterranean population are being used...
We characterized the genetic nature of beta-thalassaemia in northern Portugal. Of the 164 patients s...
The molecular basis of beta-thalassemia was investigated at the DNA level in 28 Belgians from 14 unr...
In this study, we sought to clarity the molecular basis of a dominant inherited beta-thalassemia, fo...
Mediterranean regions the most common b-tha-lassemia mutations are due to point mutations in gene re...
In this study we have carried out alpha- and beta-globin gene analysis and defined the beta-globin g...
Beta-thalassaemia, a widespread autosomal recessive disorder, occurs sporadically in Northern and We...
In this study we have carried out haplotype analysis at the beta-globin gene cluster and defined the...
Here we describe the identification of the rare -thalassemia mutation IVS-I-130 (G-
The main hereditary hemoglobin (Hb) disorder in Argentina is b-thalassemia (b-thal). Molecular studi...
The various clinical phenotypes in beta-thalassemias have stimulated the study of genetic factors th...
Thalassemia is a Mendelian inherited blood disease caused by alpha- and beta-globin gene mutations, ...
?-Thalassemia (?-thal) is present in 59% and 75% of patients with abnormal hemoglobin disorders in n...
The preliminary results of a pilot study are reported, intended as an initiation of a research plan,...
<div><p>ABSTRACT Introduction: Beta-thalassemia is caused by a deficient synthesis of the ß-chain o...