Fischer M, Hopmeier P, Lurf M, Neuwald C, Lachmann D
Wien Klin Wochenschr. 1979 Jan 19;91(2):45-8.
A case report is presented of the rare haemoglobinopathy HbS-thalassaemia, type betaS-betathal-O in a Greek family. The special diagnostic features are discussed, with particular reference to the differential diagnosis.