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Navigating highly homologous genes in a molecular diagnostic setting: a resource for clinical next-generation sequencing

Crossref DOI link: https://doi.org/10.1038/gim.2016.58

Published Print: 2016-12

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

Authors

Mandelker, Diana https://orcid.org/0000-0003-4154-0567
Schmidt, Ryan J. https://orcid.org/0000-0001-8789-9917
Ankala, Arunkanth

McDonald Gibson, Kristin https://orcid.org/0000-0002-3297-2002
Bowser, Mark

Sharma, Himanshu https://orcid.org/0000-0001-7133-6327
Duffy, Elizabeth https://orcid.org/0000-0002-3817-2145
Hegde, Madhuri

Santani, Avni https://orcid.org/0000-0003-2871-4307
Lebo, Matthew https://orcid.org/0000-0002-9733-5207
Funke, Birgit
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Text and Data Mining valid from 2016-12-01

Text and Data Mining valid from 2016-12-01

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

Article Title: Navigating highly homologous genes in a molecular diagnostic setting: a resource for clinical next-generation sequencing

Journal Title: Genetics in Medicine

CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/gim.2016.58

Content Type: article

Copyright: © 2016, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics