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A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders

Crossref DOI link: https://doi.org/10.1038/gim.2016.1

Published Print: 2016-11

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

Authors

Stark, Zornitza https://orcid.org/0000-0001-8640-1371
Tan, Tiong Y.

Chong, Belinda

Brett, Gemma R. https://orcid.org/0000-0003-0133-7994
Yap, Patrick https://orcid.org/0000-0002-3175-1136
Walsh, Maie

Yeung, Alison

Peters, Heidi

Mordaunt, Dylan https://orcid.org/0000-0002-9775-0603
Cowie, Shannon

Amor, David J.

Savarirayan, Ravi

McGillivray, George

Downie, Lilian

Ekert, Paul G. https://orcid.org/0000-0002-2976-8617
Theda, Christiane https://orcid.org/0000-0001-7577-6004
James, Paul A.

Yaplito-Lee, Joy https://orcid.org/0000-0002-6158-6215
Ryan, Monique M.

Leventer, Richard J.

Creed, Emma

Macciocca, Ivan https://orcid.org/0000-0002-0908-8542
Bell, Katrina M.

Oshlack, Alicia

Sadedin, Simon

Georgeson, Peter https://orcid.org/0000-0002-5096-4735
Anderson, Charlotte https://orcid.org/0000-0003-3310-3834
Thorne, Natalie

Gaff, Clara

White, Susan M. https://orcid.org/0000-0001-7611-634X
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Text and Data Mining valid from 2016-11-01

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This article is maintained by: Elsevier

Article Title: A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders

Journal Title: Genetics in Medicine

CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/gim.2016.1

Content Type: article

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

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