The hereditary haemolytic anaemias
Author(s)
Bibliographic Information
The hereditary haemolytic anaemias
（Haemolytic anaemias / Sir John Dacie, v.1-2）
Churchill Livingstone : Distributed in the United States of America by Churchill Livingstone, 1985-
3rd ed.
- pt. 1
- pt. 2
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Description and Table of Contents
Description
This covers the recent advances in the understanding of the medical significance of abnormal haemoglobins and thalassaemia - advances as dramatic as any in the whole field of medicine.
Table of Contents
- Sickle-cell disease, including clinical aspects, haemotological findings, screening programmes, haemoglobin S and beta-thalassaemia, the sickling phenomenon, treatment and antenatal diagnosis
- haemoglobins C, C Harlem, D, E and O
- the unstable haemoglobin
- the thalassaemias, including clinical and haematological aspects, pathology, molecular genetics, differential and antenatal diagnosis, treatment.
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