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HARVARD Citation
Cucco, F. et al. (2020). Pathogenic variants in EP300 and ANKRD11 in patients with phenotypes overlapping Cornelia de Lange syndrome. American journal of medical genetics. 182 (7), pp. 1690-1696. [Online].
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Cucco, F. et al. (2020). Pathogenic variants in EP300 and ANKRD11 in patients with phenotypes overlapping Cornelia de Lange syndrome. American journal of medical genetics. 182 (7), pp. 1690-1696. [Online].