Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study

Lord, J, McMullan, DJ, Eberhardt, RY et al. (40 more authors) (2019) Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study. The Lancet, 393 (10173). pp. 747-757. ISSN 0140-6736

Abstract

Metadata

Authors/Creators:
  • Lord, J
  • McMullan, DJ
  • Eberhardt, RY
  • Rinck, G
  • Hamilton, SJ
  • Quinlan-Jones, E
  • Prigmore, E
  • Keelagher, R
  • Best, SK
  • Carey, GK
  • Mellis, R
  • Robart, S
  • Berry, IR
  • Chandler, KE
  • Cilliers, D
  • Cresswell, L
  • Edwards, SL
  • Gardiner, C
  • Henderson, A
  • Holden, ST
  • Homfray, T
  • Lester, T
  • Lewis, RA
  • Newbury-Ecob, R
  • Prescott, K
  • Quarrell, OW
  • Ramsden, SC
  • Roberts, E
  • Tapon, D
  • Tooley, MJ
  • Vasudevan, PC
  • Weber, AP
  • Wellesley, DG
  • Westwood, P
  • White, H
  • Parker, M
  • Williams, D
  • Jenkins, L
  • Scott, RH
  • Kilby, MD
  • Chitty, LS
  • Hurles, ME
  • Maher, ER
Copyright, Publisher and Additional Information: © 2019 The Author(s). Published by Elsevier Ltd. This is an open access article under the terms of the Creative Commons Attribution 4.0 International (CC BY 4.0) (https://creativecommons.org/licenses/by/4.0/)
Dates:
  • Published: 23 February 2019
  • Published (online): 31 January 2019
Institution: The University of Leeds
Academic Units: 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: 14 Feb 2020 10:29
Last Modified: 14 Feb 2020 10:29
Status: Published
Publisher: Elsevier
Identification Number: https://doi.org/10.1016/s0140-6736(18)31940-8

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