1. Milder variant of sickle-cell disease in Arabs in Kuwait associated with unusually high level of fetal haemoglobin;Ali, S.A.;British Journal ofHaematology,1970
2. Irreversibly sickled erythrolytes: a consequence of the heterogeneous distribution of haemoglobin types in sickle-cell anemia;Bertles, J.F.; Milner, P.F.;Journal of Clinical Investigation,1968
3. Rate of sickling of red cells during deoxygenation of blood from persons with various sickling disorders;Charache, S.; Conley, C.L.;Blood,1964
4. Prolonged survival of a patient with sickle-cell anemia;Charache, S.; Richardson, S.M.;Archives of Internal Medicine,1964
5. Abnormal human haemoglobins. Separation and characterisation of the a and chains by chromatography, and the determination of two new variants, Hb Chesapeake and Hb;Clegg, J.B.; Naughton, M.A.; Weatherall, D.J.;J. Bangkok. Journal of Molecular Biology,1966