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Contents of Volume
Inheritance of haemoglobin S
Homozygous sicklecell disease HbSS disease
11 other sections not shown
abnormal haemoglobin Acad acid Acta haemat adult Amer anaemic associated Basel blood films blood picture bone marrow Brit chains Charache Clegg clin clinical co-workers compound heterozygotes concentration concluded Cooley's crisis deletion demonstrated deoxygenated described diagnosis Diggs effect electrophoresis erythrocytes erythropoiesis fetal g/dl genetic genotype globin globin gene haem haematological haemo haemoglobin haemoglobinopathy haemolysis haemolytic anaemia haplotype Hb A2 Hb Bart's Hb F Hb-AA Hb-F percentage Hb-H Hb-S Hb-SC Hb-SS cells Hb-SS disease Hb-SS patients Heinz bodies heterozygous homozygotes homozygous HPFH Huisman infants infarction infection iron ISCs Lehmann liver membrane mild molecular Nature Lond normal oxygen P-globin plasma platelet present red cell reported result reticulocyte count Serjeant serum severe sickle cell anemia sickle cell disease sickle-cell anaemia sickle-cell disease sickle-cell trait spleen splenectomy splenic studied symptoms syndrome synthesis thalassaemia thalassaemia major transfusion unstable haemoglobin variant vaso-occlusive vitro Weatherall