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HARVARD Citation
Gall, B. et al. (2022). Assessment of an automated approach for variant interpretation in screening for monogenic disorders: A single‐center study. Molecular genetics & genomic medicine. 10 (12), p. n/a. [Online].
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Gall, B. et al. (2022). Assessment of an automated approach for variant interpretation in screening for monogenic disorders: A single‐center study. Molecular genetics & genomic medicine. 10 (12), p. n/a. [Online].