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Whole genome sequencing reveals that genetic conditions are frequent in intensively ill children

Crossref DOI link: https://doi.org/10.1007/s00134-019-05552-x

Published Online: 2019-03-07

Published Print: 2019-05

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

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French, Courtney E.

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Delon, Isabelle

Dolling, Helen

Sanchis-Juan, Alba

Shamardina, Olga

Mégy, Karyn

Abbs, Stephen

Austin, Topun

Bowdin, Sarah

Branco, Ricardo G.

Firth, Helen

Rowitch, David H.

Raymond, F. Lucy http://orcid.org/0000-0003-2652-3355
Funding

Funding for this research was provided by:

Rosetree Trust (N/A)

NIHR Bioresource (RG65966)

NIHR Biomedical Research Centre (2017-2022)
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Article History

Received: 8 November 2018

Accepted: 28 January 2019

First Online: 7 March 2019

Compliance with ethical standards

:

: The author(s) declare that they have no conflicts of interest.

: Participants for this study were recruited through NHS Cambridge University Hospitals Foundation Trust under Cambridge South Research Ethics Committee approval 13/EE/0325.