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HARVARD Citation
Lebrun, N. et al. (2018). Molecular and cellular issues of KMT2A variants involved in Wiedemann-Steiner syndrome. European journal of human genetics. pp. 107-116. [Online].
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Lebrun, N. et al. (2018). Molecular and cellular issues of KMT2A variants involved in Wiedemann-Steiner syndrome. European journal of human genetics. pp. 107-116. [Online].