Fetal hemoglobin levels in sickle cell disease and normal individuals are partially controlled by an X-linked gene located at Xp22.2

G. J. Dover, K. D. Smith, Y. C. Chang, S. Purvis, A. Mays, D. A. Meyers, C. Sheils, G. Serjeant

Research output: Contribution to journal › Article › peer-review

160 Scopus citations

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