Severity differences in β-thalassaemia/haemoglobin E syndromes: implication of genetic factors
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1993.tb04702.x/fullpdf
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1. Globin Chain Electrophoresis: a New Approach to the Determination of theGγ/Aγ Ratio in Fetal Haemoglobin and to Studies of Globin Synthesis
2. Nonrandom association of polymorphic restriction sites in the -globin gene cluster
3. Production of F cells in sickle cell anemia: regulation by a genetic locus or loci separate from the beta-globin gene cluster
4. Interaction between Homozygous β0Thalassaemia and the Swiss Type of Hereditary Persistence of Fetal Haemoglobin
5. Variation in hemoglobin F production among normal and sickle cell adults is not related to nucleotide substitutions in the gamma promoter regions
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