Erythrocytapheresis for chronically transfused children with sickle cell disease: an effective method for maintaining a low hemoglobin S level and reducing iron overload. [electronic resource]

By: Contributor(s): Producer: 19991221Description: 122-5 p. digitalISSN:
  • 0733-2459
Subject(s): Online resources: In: Journal of clinical apheresis vol. 14
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Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S.

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