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Elsevier, Genetics in Medicine, 11(21), p. 2504-2511, 2019

DOI: 10.1038/s41436-019-0518-x

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Variant recurrence in neurodevelopmental disorders: the use of publicly available genomic data identifies clinically relevant pathogenic missense variants

This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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