The hereditary haemolytic anaemias.

Abstract

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.