论文信息 - The Abnormal Haemoglobins in Homozygous α‐Thalassaemia

The Abnormal Haemoglobins in Homozygous α‐Thalassaemia

Summary The red cells from Chinese stillborn infants with erythroblastosis foetalis due to homozygous α‐thalassaemia contain about 80% Hb‐γ4, the second haemoglobin always present does not contain α‐chains and has the structure Hbγ2X2 identical to Hb‐Portland 1. Hb‐A, Hb‐F, or Hb‐A2 were not detected.

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