The Ratio of the ^Gγ and ^Aγ Chains: Variations due to Anomalies at the Molecular Level

This publication has 24 references indexed in Scilit:

• Restriction endonuclease maps of the β-like globin gene cluster in the British and Greek forms of HPFH, and for one example of Gγβ+ HPFH
  British Journal of Haematology, 2008
• Dutch β°‐thalassaemia: a 10 kilobase DNA deletion associated with significant γ‐chain production
  British Journal of Haematology, 1984
• The occurrence of different levels ofGγ chain and of theAγT variant of fetal hemoglobin in newborn babies from several countries
  American Journal of Hematology, 1983
• Linkage of β-thalassaemia mutations and β-globin gene polymorphisms with DNA polymorphisms in human β-globin gene cluster
  Nature, 1982
• Linkage Analysis of Nondeletion Hereditary Persistence of Fetal Hemoglobin
  Science, 1982
• Human fetal gγ- and Aγ-globin genes: Complete nucleotide sequences suggest that DNA can be exchanged between these duplicated genes
  Cell, 1980
• The chemical heterogeneity of the fetal hemoglobin in normal newborn infants and in adults
  Molecular and Cellular Biochemistry, 1977
• Heterocellular Hereditary Persistence of Fetal Haemoglobin (Heterocellular HPFH) and its Interaction with β Thalassaemia
  British Journal of Haematology, 1977
• Another Form of tie Hereditary Persistence of Fetal Hemoglobin (The Atlanta Type)?
  Hemoglobin, 1976
• BENIGN SICKLE-CELL ANÆMIA
  The Lancet, 1972