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HARVARD Citation
Sun, Y. et al. (2017). Further delineation of the phenotype of truncating KMT2A mutations: The extended Wiedemann–Steiner syndrome. American journal of medical genetics. 173 (2), pp. 510-514. [Online].
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Sun, Y. et al. (2017). Further delineation of the phenotype of truncating KMT2A mutations: The extended Wiedemann–Steiner syndrome. American journal of medical genetics. 173 (2), pp. 510-514. [Online].