The α-Globin Genotype as a Determinant of Hematologic Parameters in Sickle Cell Trait

This publication has 16 references indexed in Scilit:

• Organization of the alpha-globin genes in the Chinese alpha-thalassemia syndromes.
  Journal of Clinical Investigation, 1979
• The duplicated human alpha globin genes lie close together in cellular DNA.
  Proceedings of the National Academy of Sciences, 1978
• Competition of normal β chains and sickle haemoglobin β chains for α chains as a post-translational control mechanism
  Nature, 1978
• Evidence for Rapid Loss of Newly Synthesized Haemoglobin S Molecules in Sickle Cell Anaemia and Sickle Cell Trait
  British Journal of Haematology, 1977
• Differences in Affinity of Variant β Chains for a Chains: A Possible Explanation for the Variation in the Percentages of β Chain Variants in Heterozygotes
  Hemoglobin, 1977
• Trimodality in Tie Percentages of β Chain Variants in Heterozy-Gotes: The Effect of the Number of Aczive HB_αStructural Loci
  Hemoglobin, 1977
• Trimodality in the proportion of hemoglobin G Philadelphia in heterozygotes: evidence for heterogeneity in the number of human alpha chain loci.
  Proceedings of the National Academy of Sciences, 1976
• Studies on the Proportion and Synthesis of Haemoglobin G Philadelphia in Red Cells of Heterozygotes, a Homozygote, and a Heterozygote for both Haemoglobin G and α Thalassaemia
  British Journal of Haematology, 1976
• The Interaction of α-Thalassaemia and Haemoglobin G Philadelphia
  British Journal of Haematology, 1976
• Preferential Binding of βS Globin Chains Associated with Stroma in Sickle Cell Disorders
  Journal of Clinical Investigation, 1974