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  3. Use of SNP chips to detect rare pathogenic variants: retrospective, population based diagnostic evaluation
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Corrections

Use of SNP chips to detect rare pathogenic variants: retrospective, population based diagnostic evaluation

BMJ 2021; 372 doi: https://doi.org/10.1136/bmj.n792 (Published 22 March 2021) Cite this as: BMJ 2021;372:n792

This paper by Weedon and colleagues (BMJ 2021;372:n214, doi:10.1136/bmj.n214) should have a CC-BY open access licence rather than the CC-BY-NC licence with which it was originally published. The online version has been amended.

http://creativecommons.org/licenses/by/4.0/

This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/.

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