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Identification of clinically actionable variants from genome sequencing of families with congenital heart disease

Crossref DOI link: https://doi.org/10.1038/s41436-018-0296-x

Published Print: 2019-05

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

Authors

Alankarage, Dimuthu

Ip, Eddie

Szot, Justin O.

Munro, Jacob

Blue, Gillian M.

Harrison, Katrina

Cuny, Hartmut

Enriquez, Annabelle

Troup, Michael

Humphreys, David T.

Wilson, Meredith

Harvey, Richard P.

Sholler, Gary F.

Graham, Robert M.

Ho, Joshua W.K.

Kirk, Edwin P.

Pachter, Nicholas

Chapman, Gavin

Winlaw, David S.

Giannoulatou, Eleni

Dunwoodie, Sally L.
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Text and Data Mining valid from 2019-05-01

Text and Data Mining valid from 2019-05-01

Version of Record valid from 2022-01-19
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This article is maintained by: Elsevier

Article Title: Identification of clinically actionable variants from genome sequencing of families with congenital heart disease

Journal Title: Genetics in Medicine

CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-018-0296-x

Content Type: article

Copyright: © 2019, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics