The distribution of fetal hemoglobin and the types of γ chain in red cell fractions separated by gradient centrifugation from blood of patients with sickle cell anemia and other hemoglobinopathies
Author:
Publisher
Elsevier BV
Subject
Biochemistry
Reference28 articles.
1. THE PRESENT STATUS OF THE HETEROGENEITY OF FETAL HEMOGLOBIN IN ?-THALASSEMIA: AN ATTEMPT TO UNIFY SOME OBSERVATIONS IN THALASSEMIA AND RELATED CONDITIONS
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3. Cellular and Molecular Regulation of Hemoglobin Switching;Schroeder,1979
4. Recent advances in the quantitation of human fetal hemoglobins with different gamma chains
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1. FORTY-FOUR YEARS (1955–1999) DEVOTED TO HEMOGLOBIN RESEARCH: TITUS H. J. HUISMAN (1923–1999);Hemoglobin;2001-01
2. Hb Costa Rica or α2β277(EF1)His→Arg: The first example of a somatic cell mutation in a globin gene;Human Genetics;1996-06
3. Hb Costa Rica or · 2 ‚ 2 77(EF1)His→Arg: the first example of a somatic cell mutation in a globin gene;Human Genetics;1996-05-02
4. Hematological Observations on Arabian SS Patients with a Homozygosity or Heterozygosity for a βSChromosome with Haplotype #31;Hemoglobin;1985-01
5. Heterogeneity in the molecular basis of three types of hereditary persistence of fetal hemoglobin and the relative synthesis of the G? and A? types of ? chain;Biochemical Genetics;1984-02
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