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. 2021 Mar 22;372:n792. doi: 10.1136/bmj.n792

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

PMCID: PMC7983866  PMID: 33753354

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.


Articles from The BMJ are provided here courtesy of BMJ Publishing Group

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