Association of thalassaemia intermedia with a beta-globin gene haplotype
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1987.tb06870.x/fullpdf
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4. A point mutation in the Aγ-globin gene promoter in Greek hereditary persistence of fetal haemoglobin
5. G to A substitution in the distal CCAAT box of the Aγ-globin gene in Greek hereditary persistence of fetal haemoglobin
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