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HARVARD Citation
Song, H. et al. (n.d.). A case report of de novo missense FOXP1 mutation in a non‐Caucasian patient with global developmental delay and severe speech impairment. Clinical case reports. 3 (2), pp. 110-113. [Online].
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Song, H. et al. (n.d.). A case report of de novo missense FOXP1 mutation in a non‐Caucasian patient with global developmental delay and severe speech impairment. Clinical case reports. 3 (2), pp. 110-113. [Online].