BENIGN SICKLE-CELL ANÆMIA
- 1 December 1972
- journal article
- Published by Elsevier in The Lancet
- Vol. 300 (7788), 1163-1167
- https://doi.org/10.1016/s0140-6736(72)92592-5
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Irreversibly Sickled Cells and Splenomegaly in Sickle‐Cell AnaemiaBritish Journal of Haematology, 1970
- Sickle Cell Disease in Saudi ArabsActa Haematologica, 1970
- A New Sickling Disorder Resulting from Interaction of the Genes for Haemoglobin S and α‐ThalassaemiaBritish Journal of Haematology, 1969
- Haemoglobin F(Malta): a New Foetal Haemoglobin Variant with a High Incidence in Maltese InfantsNature, 1969
- The Pattern of Disordered Haemoglobin Synthesis in Homozygous and Heterozygous β-ThalassaemiaBritish Journal of Haematology, 1969
- Irreversibly sickled erythrocytes: a consequence of the heterogeneous distribution of hemoglobin types in sickle-cell anemiaJournal of Clinical Investigation, 1968
- Relatively Benign Sickle-cell Anaemia in 60 Patients Aged Over 30 in the West IndiesBMJ, 1968
- Compensation in Haemolytic Anaemias caused by Abnormal HaemoglobinsNature, 1968
- Glucose-6-phosphate dehydrogenase deficiency, the sickling trait, and malaria in Saudi Arab childrenThe Journal of Pediatrics, 1967
- Abnormal human haemoglobins: Separation and characterization of the α and β chains by chromatography, and the determination of two new variants, Hb chesapeake and Hb J (Bangkok)Journal of Molecular Biology, 1966