Sickle Cell-Hemoglobin D Iran: A Benign Sickle Cell Syndrome by Serjeant, B, Myerscough, E, Serjeant, G, Higgs, D, Moo-Penn, W

The changing face of homozygous sickle cell disease: 102 patients over 60 years. by Serjeant, G, Serjeant, B, Mason, K, Hambleton, I, Fisher, C, Higgs, D

The interaction of alpha thalassaemia and sickle cell-beta zero thalassaemia. by Vyas, P, Higgs, D, Weatherall, D, Dunn, D, Serjeant, B, Serjeant, G

Hb S-β-thalassemia: molecular, hematological and clinical comparisons. by Serjeant, G, Serjeant, B, Fraser, R, Hambleton, I, Higgs, D, Kulozik, A, Donaldson, A

The red cell distribution width in sickle cell disease--is it of clinical value? by Thame, M, Grandison, Y, Mason, K, Thompson, M, Higgs, D, Morris, J, Serjeant, B, Serjeant, G

The haematology of homozygous sickle cell disease after the age of 40 years by Morris, J, Dunn, D, Beckford, M, Grandison, Y, Mason, K, Higgs, D, Ceulaer, K, Serjeant, B, Serjeant, G