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Using high-resolution variant frequencies to empower clinical genome interpretation

Crossref DOI link: https://doi.org/10.1038/gim.2017.26

Published Print: 2017-10

Update policy: https://doi.org/10.1016/elsevier_cm_policy

Authors

Whiffin, Nicola

Minikel, Eric

Walsh, Roddy

O’Donnell-Luria, Anne H

Karczewski, Konrad

Ing, Alexander Y

Barton, Paul J R

Funke, Birgit

Cook, Stuart A

MacArthur, Daniel

Ware, James S
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Text and Data Mining valid from 2017-10-01

Text and Data Mining valid from 2017-10-01

Version of Record valid from 2021-11-24
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This article is maintained by: Elsevier

Article Title: Using high-resolution variant frequencies to empower clinical genome interpretation

Journal Title: Genetics in Medicine

CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/gim.2017.26

Content Type: article

Copyright: © 2017, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics