An alternative to array-based diagnostics: a prospectively recruited cohort, comparing arrayCGH to next-generation sequencing to evaluate foetal structural abnormalities

Walker, L, Watson, CM orcid.org/0000-0003-2371-1844, Hewitt, S et al. (3 more authors) (2019) An alternative to array-based diagnostics: a prospectively recruited cohort, comparing arrayCGH to next-generation sequencing to evaluate foetal structural abnormalities. Journal of Obstetrics and Gynaecology, 39 (3). pp. 328-334. ISSN 0144-3615

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Copyright, Publisher and Additional Information: © 2019 Informa UK Limited, trading as Taylor & Francis Group. This is an author produced version of a paper published in the Journal of Obstetrics and Gynaecology. Uploaded in accordance with the publisher's self-archiving policy.
Keywords: Next-generation sequencing; copy number variation; foetal structural anomaly
Dates:
  • Published: 3 April 2019
  • Accepted: 9 September 2018
  • Published (online): 3 February 2019
Institution: The University of Leeds
Academic Units: The University of Leeds > Faculty of Medicine and Health (Leeds) > School of Medicine (Leeds) > Inst of Biomed & Clin Sciences (LIBACS) (Leeds) > Genetics (LIBACS) (Leeds)
The University of Leeds > Faculty of Medicine and Health (Leeds) > Institute of Molecular Medicine (LIMM) (Leeds) > Section of Opthalmology and Neurosciences (Leeds)
Depositing User: Symplectic Publications
Date Deposited: 15 May 2019 14:08
Last Modified: 04 Jun 2019 10:31
Status: Published
Publisher: Taylor & Francis
Identification Number: https://doi.org/10.1080/01443615.2018.1522529
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Embargoed until: 3 February 2020

Filename: CNVseq April 2018.pdf

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