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Diagnosis of fetal abnormalities using exome sequencing: translating research into practice.

Dempsey, E; Pryce, J; Thilaganathan, B; Mansour, S; Homfray, T; Drury, S (2020) Diagnosis of fetal abnormalities using exome sequencing: translating research into practice. Ultrasound Obstet Gynecol, 56 (5). p. 779. ISSN 1469-0705 https://doi.org/10.1002/uog.21959
SGUL Authors: Thilaganathan, Baskaran

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Item Type: Article
Additional Information: This is the peer reviewed version of the following article: Dempsey, E., Pryce, J., Thilaganathan, B., Mansour, S., Homfray, T. and Drury, S. (2020), Diagnosis of fetal abnormalities using exome sequencing: translating research into practice. Ultrasound Obstet Gynecol, 56: 779-779, which has been published in final form at https://doi.org/10.1002/uog.21959. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.
Keywords: Prenatal diagnosis, exome sequencing Fetal Hydrops, genomics, 1114 Paediatrics and Reproductive Medicine, Obstetrics & Reproductive Medicine
SGUL Research Institute / Research Centre: Academic Structure > Molecular and Clinical Sciences Research Institute (MCS)
Journal or Publication Title: Ultrasound Obstet Gynecol
ISSN: 1469-0705
Language: eng
Dates:
DateEvent
2 November 2020Published
25 December 2019Published Online
13 December 2019Accepted
Publisher License: Publisher's own licence
PubMed ID: 31875334
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/111529
Publisher's version: https://doi.org/10.1002/uog.21959

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