Hb S(C)-β+-thalassaemia: different mutations are associated with different levels of normal Hb A
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1988.tb02438.x/fullpdf
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1. Haplotypes and levels of fetal hemoglobin andGγ toAγ ratios in mediterranean patients with thalassemia minor and major
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4. β+ Thalassemia: Aberrant splicing results from a single point mutation in an intron
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