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HARVARD Citation
Vears, D. et al. (2018). How do consent forms for diagnostic high‐throughput sequencing address unsolicited and secondary findings? A content analysis. Clinical genetics. 94 (3), pp. 321-329. [Online].
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Vears, D. et al. (2018). How do consent forms for diagnostic high‐throughput sequencing address unsolicited and secondary findings? A content analysis. Clinical genetics. 94 (3), pp. 321-329. [Online].