Now showing items 1-10 of 455
Molecular identification of Sicilian (deltaß)º-thalassemia associated with ß-thalassemia and hemoglobin S in Brazil
(Associação Brasileira de Divulgação Científica, 2002)
Molecular identification of Sicilian (8 beta)degrees-thalassemia associated with beta-thalassemia and hemoglobin S in Brazil
(Assoc Bras Divulg CientificaSao PauloBrasil, 2002)
HFE gene mutations in Brazilian thalassemic patients
Hereditary hemochromatosis is a disorder of iron metabolism characterized by increased iron intake and progressive storage and is related to mutations in the HFE gene. Interactions between thalassemia and hemochromatosis ...
Thalassemia intermedia as a result of heterozygosis for beta(0)-thalassemia and alpha alpha alpha(anti-3.7)/alpha alpha genotype in a Brazilian patient
(Assoc Bras Divulg CientificaSao PauloBrasil, 2003)
Camperdown hemoglobin associated with beta degrees thalassemia in a Brazilian child
(Soc Brasil GeneticaRibeirao PretBrasil, 2005)
Evaluation of HPFH and δβ-thalassemia mutations in a Brazilian group with high Hb F levels.
Fetal hemoglobin (Hb F) is characteristic of the fetal development period. However, in some genetic conditions, such as hereditary persistence of fetal hemoglobin (HPFH) and delta-beta thalassemia (δβ-thalassemia), Hb F ...
Thalassemia intermedia as a result of heterozygosis for ß0-thalassemia and aaaanti-3.7/aa genotype in a Brazilian patient
(Associação Brasileira de Divulgação Científica, 2003)
A new beta(0)-thalassemia frameshift mutation [beta 48 (-T)] in a Uruguayan family