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HARVARD Citation
van den Akker, W. et al. (2018). De novo variants in CDK13 associated with syndromic ID/DD: Molecular and clinical delineation of 15 individuals and a further review. Clinical genetics. 93 (5), pp. 1000-1007. [Online].
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van den Akker, W. et al. (2018). De novo variants in CDK13 associated with syndromic ID/DD: Molecular and clinical delineation of 15 individuals and a further review. Clinical genetics. 93 (5), pp. 1000-1007. [Online].