Clinical, haematological, and genetic studies of type 2 normal Hb A2 beta thalassaemia.

Lignende værker

• Clinical and haematological evaluation of beta thalassaemia intermedia with increased Hb F and Hb A2 in heterozygotes: beta thalassaemia intermedia I.
  af: Altay, C, et al.
  Udgivet: (1985)
• Clinical and haematological evaluation of beta thalassaemia intermedia characterised by unusually low Hb F and increased Hb A2: beta thalassaemia intermedia II.
  af: Gurgey, A, et al.
  Udgivet: (1985)
• Beta-thalassaemia, G-6-PD deficiency, and atypical cholinesterase in Cyprus.
  af: Kattamis, C, et al.
  Udgivet: (1972)
• Serum iron and unsaturated iron-binding capacity in the -thalassaemia trait: their relation to the levels of haemoglobins A, A 2 , and F.
  af: Kattamis, C, et al.
  Udgivet: (1972)
• A genetic combination of silent beta-thalassaemia, high Hb A2 beta-thalassaemia, and single alpha globin gene deletion causing mild thalassaemia intermedia.
  af: Galanello, R, et al.
  Udgivet: (1984)