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Regulation of human alpha-globin gene expression and alpha-thalassemia
(Funpec-editoraRibeirao PretoBrasil, 2008)
Screening for mutations in human alpha-globin genes by nonradioactive single-strand conformation polymorphism
(Associação Brasileira de Divulgação Científica, 2003)
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)
Hemoglobin H disease resulting from the association of the - alpha(3.7) rightward deletion and the (alpha alpha)(MM) deletion in a Brazilian patient
(Blackwell MunksgaardCopenhagenDinamarca, 2002)
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 ...
alpha-Globin genes: thalassemic and structural alterations in a Brazilian population
(Associação Brasileira de Divulgação Científica, 2000)