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Tharreau, M. et al. (2022). Refining the clinical phenotype associated with missense variants in exons 38 and 39 of KMT2D. American journal of medical genetics. 188 (5), pp. 1600-1606. [Online].
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Tharreau, M. et al. (2022). Refining the clinical phenotype associated with missense variants in exons 38 and 39 of KMT2D. American journal of medical genetics. 188 (5), pp. 1600-1606. [Online].