B C Kar

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  • B C Kar, R K Satapathy, A E Kulozik, M Kulozik, S Sirr, B E Serjeant +1 other
  • 1986
A study of 131 patients with homozygous sickle cell (SS) disease in Orissa State, India, indicated that, compared with Jamaican patients, Indian patients have higher frequencies of alpha thalassaemia, higher fetal haemoglobin, total haemoglobin, and red cell counts, and lower mean cell volume, mean cell haemoglobin concentration, and reticulocyte counts.(More)
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