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Copy-number variants in clinical genome sequencing: deployment and interpretation for rare and undiagnosed disease

Crossref DOI link: https://doi.org/10.1038/s41436-018-0295-y

Published Print: 2019-05

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

Authors

Gross, Andrew M.

Ajay, Subramanian S.

Rajan, Vani

Brown, Carolyn

Bluske, Krista

Burns, Nicole J.

Chawla, Aditi

Coffey, Alison J.

Malhotra, Alka

Scocchia, Alicia

Thorpe, Erin

Dzidic, Natasa

Hovanes, Karine

Sahoo, Trilochan

Dolzhenko, Egor

Lajoie, Bryan

Khouzam, Amirah

Chowdhury, Shimul

Belmont, John

Roller, Eric

Ivakhno, Sergii

Tanner, Stephen

McEachern, Julia

Hambuch, Tina

Eberle, Michael

Hagelstrom, R. Tanner

Bentley, David R.

Perry, Denise L.

Taft, Ryan J.
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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 2021-11-24
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This article is maintained by: Elsevier

Article Title: Copy-number variants in clinical genome sequencing: deployment and interpretation for rare and undiagnosed disease

Journal Title: Genetics in Medicine

CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-018-0295-y

Content Type: article

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