The Clinical and Biosynthetic Characterization of αβ-Thalassaemia
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1972.tb05695.x/fullpdf
Reference39 articles.
1. Estimation of Small Percentages of Fœtal Hæmoglobin
2. Abnormal human haemoglobins
3. Haemoglobin Synthesis in α-Thalassaemia (Haemoglobin H Disease)
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3. Epistatic interactions between genetic disorders of hemoglobin can explain why the sickle-cell gene is uncommon in the Mediterranean;Proceedings of the National Academy of Sciences;2009-12-01
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