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HARVARD Citation
Miyake, N. et al. (2016). Delineation of clinical features in Wiedemann–Steiner syndrome caused by KMT2A mutations. Clinical genetics. 89 (1), pp. 115-119. [Online].
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Miyake, N. et al. (2016). Delineation of clinical features in Wiedemann–Steiner syndrome caused by KMT2A mutations. Clinical genetics. 89 (1), pp. 115-119. [Online].