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Evaluation of HPFH and δβ-thalassemia mutations in a Brazilian group with high Hb F levels.
(2011-12-01)
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 ...
Evaluation of HPFH and δβ-thalassemia mutations in a Brazilian group with high Hb F levels.
(2011-12-01)
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 ...
Influence of δβ-thalassemia or regulatory elements in individuals with increased fetal Hb levels in the São Paulo northwest population
(2011-11-16)
Fetal hemoglobin (Hb F), formed by two alpha globin chains (α) and two gamma chains (γ) (α2 γ2), has reduced expression in adults, ranging from 0 to 1% of total hemoglobin. Increased levels of Hb F are due to mutations in ...
Influence of δβ-thalassemia or regulatory elements in individuals with increased fetal Hb levels in the São Paulo northwest population
(2011-11-16)
Fetal hemoglobin (Hb F), formed by two alpha globin chains (α) and two gamma chains (γ) (α2 γ2), has reduced expression in adults, ranging from 0 to 1% of total hemoglobin. Increased levels of Hb F are due to mutations in ...
Identification of novel candidate genes for globin regulation in erythroid cells containing large deletions of the human beta-globin gene cluster
(Academic Press Inc Elsevier ScienceSan DiegoEUA, 2006)
Dificuldades no diagnóstico laboratorial das hemoglobinopatias
(2007-07-01)
There are various types of hemoglobinopathies that are characterized by variants of abnormal hemoglobins (eg. Hb S, HbC, unstables Hb, etc.) and thalassemias (eg. alpha, beta, beta/delta, etc.). Hemoglobinopathies account ...
Dificuldades no diagnóstico laboratorial das hemoglobinopatias
(Associação Brasileira de Hematologia e Hemoterapia e daSociedade Brasileira de Transplante de Medula Óssea, 2007-09-01)
Há vários tipos de hemoglobinopatias que são caracterizados por variantes das hemoglobinas anormais (ex: Hb S, Hb C, Hb Instáveis,etc) e por talassemias (ex: tal. alfa, tal. beta, tal.beta/delta,etc) As hemoglobinopatias ...
Dificuldades no diagnóstico laboratorial das hemoglobinopatias
(Associação Brasileira de Hematologia e Hemoterapia e daSociedade Brasileira de Transplante de Medula Óssea, 2014)