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    A rare gene variation cap +1 (A>C) (HBB: c. −50A>C) associated with codon 5 (‐CT) (HBB: c.17_18delCT) mutation in Syrian family
    by Hossam Murad, Faten Moassas, Nour A. L. Fakseh
    Published 2021-03-01
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    Article
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