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Contents of Volume
Inheritance of haemoglobin S
Homozygous sicklecell disease HbSS disease
11 other sections not shown
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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