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HARVARD Citation
Veerappa, A. et al. (2014). Family based genome‐wide copy number scan identifies complex rearrangements at 17q21.31 in dyslexics. American journal of medical genetics. 165 (7), pp. 572-580. [Online].
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Veerappa, A. et al. (2014). Family based genome‐wide copy number scan identifies complex rearrangements at 17q21.31 in dyslexics. American journal of medical genetics. 165 (7), pp. 572-580. [Online].