Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)alpha-Thalassemia, arising from a defect in alpha-globin chain synthesis, is often caused by deletions involving one or both of the alpha-genes on the same allele. With the aim of investigating the prevalence of alpha-thalassemia 3.7 kb deletion in the adult population of Rio Grande do Norte, 713 unrelated individuals, between 18 and 59 years-of-age, were analyzed. Red blood cell indices were electronically determined, and A(2) and F hemoglobins evaluated by HPLC. PCR was applied to the molecular investigation of alpha-thalassemia 3.7 kb deletion. Eighty (11.2%) of the 713 individuals investigated presented alpha-...
Alpha-thalassemia is the most common inherited disorder of hemoglobin synthesis. Genomic deletions i...
Abstract Alpha-thalassemias are among the most common genetic diseases in the world. They are charac...
IntroductionCases with microcytosis not responding adequately to iron supplementation are diagnostic...
α-Thalassemia, arising from a defect in a-globin chain synthesis, is often caused by deletions ...
-Thalassemia, arising from a defect in -globin chain synthesis, is often caused by deletions involvi...
α-Thalassemia, arising from a defect in a-globin chain synthesis, is often caused by deletions invol...
Alpha thalassemia has not been systematically investigated in Brazil. In this study, 493 unrelated i...
Alpha thalassemia, the most common monogenic disorder in the world, is characterized by deletions o...
Alpha thalassemia has not been systematically investigated in Brazil. In this study, 493 unrelated i...
ABSTRACT. The ethnic composition of the Brazilian popula-tion favors high frequencies of the-α3.7 de...
Alpha thalassemia has not been systematically investigated in Brazil. In this study, 493 unrelated i...
Alpha-thalassemia (α-thal) is one of the most common monogenic disorders in the world. Its clinical ...
In order to determine the contribution of alpha-thalassemia to microcytosis and hypochromia, 339 adu...
Seven unrelated patients with hemoglobin (Hb) H disease and 27 individuals with alpha-chain structur...
Seven unrelated patients with hemoglobin (Hb) H disease and 27 individuals with alpha-chain structur...
Alpha-thalassemia is the most common inherited disorder of hemoglobin synthesis. Genomic deletions i...
Abstract Alpha-thalassemias are among the most common genetic diseases in the world. They are charac...
IntroductionCases with microcytosis not responding adequately to iron supplementation are diagnostic...
α-Thalassemia, arising from a defect in a-globin chain synthesis, is often caused by deletions ...
-Thalassemia, arising from a defect in -globin chain synthesis, is often caused by deletions involvi...
α-Thalassemia, arising from a defect in a-globin chain synthesis, is often caused by deletions invol...
Alpha thalassemia has not been systematically investigated in Brazil. In this study, 493 unrelated i...
Alpha thalassemia, the most common monogenic disorder in the world, is characterized by deletions o...
Alpha thalassemia has not been systematically investigated in Brazil. In this study, 493 unrelated i...
ABSTRACT. The ethnic composition of the Brazilian popula-tion favors high frequencies of the-α3.7 de...
Alpha thalassemia has not been systematically investigated in Brazil. In this study, 493 unrelated i...
Alpha-thalassemia (α-thal) is one of the most common monogenic disorders in the world. Its clinical ...
In order to determine the contribution of alpha-thalassemia to microcytosis and hypochromia, 339 adu...
Seven unrelated patients with hemoglobin (Hb) H disease and 27 individuals with alpha-chain structur...
Seven unrelated patients with hemoglobin (Hb) H disease and 27 individuals with alpha-chain structur...
Alpha-thalassemia is the most common inherited disorder of hemoglobin synthesis. Genomic deletions i...
Abstract Alpha-thalassemias are among the most common genetic diseases in the world. They are charac...
IntroductionCases with microcytosis not responding adequately to iron supplementation are diagnostic...