Sickle Cell-Hemoglobin D Iran: A Benign Sickle Cell Syndrome

Παρόμοια τεκμήρια

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  ανά: Serjeant, G, κ.ά.
  Έκδοση: (2007)
• The interaction of alpha thalassaemia and sickle cell-beta zero thalassaemia.
  ανά: Vyas, P, κ.ά.
  Έκδοση: (1988)
• Are there clinical phenotypes of homozygous sickle cell disease?
  ανά: Alexander, N, κ.ά.
  Έκδοση: (2004)
• The red cell distribution width in sickle cell disease--is it of clinical value?
  ανά: Thame, M, κ.ά.
  Έκδοση: (1991)
• The changing face of homozygous sickle cell disease: 102 patients over 60 years.
  ανά: Serjeant, G, κ.ά.
  Έκδοση: (2009)