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Publications by G.R. Serjeant
Foetal Haemoglobin in Homozygous Sickle Cell Disease: A Study of Patients With Low HBF Levels*
Clinical and Laboratory Haematology
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Indices of Iron Status Are Nearer to Normal Levels in Foetal Haemoglobin Persistent Sickle Cell Anaemia Compared to the Sickle Cell Anaemia With Low Foetal Haemoglobin
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Renal Function in Patients Over 40 With Homozygous Sickle-Cell Disease.
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Significantly Elevated Foetal Haemoglobin Levels in Individuals With Glucose 6-Phosphate Dehydrogenase Disease and/or Sickle Cell Trait: A Cross-Sectional Study in Cape Coast, Ghana
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Gall Stones in Homozygous Sickle Cell Disease.
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Sickle-Cell Haemoglobin O Disease in a Sudanese Family.
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Elevated Fetal Haemoglobin Levels Are Associated With Decreased Incidence of Retinopathy in Adults With Sickle Cell Disease
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Delayed Adolescent Growth in Homozygous Sickle Cell Disease.
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