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Exome sequencing in the assessment of congenital malformations in the fetus and neonate

Authors

  • Fionnuala Mone Department of Clinical Genetics, Birmingham Women’s and Children’s NHS Foundation Trust, Birmingham, UK West Midlands Fetal Medicine Centre, Birmingham Women’s and Children’s NHS Foundation Trust, Birmingham, UK PubMed articlesGoogle scholar articles
  • Elizabeth Quinlan-Jones Department of Clinical Genetics, Birmingham Women’s and Children’s NHS Foundation Trust, Birmingham, UK West Midlands Fetal Medicine Centre, Birmingham Women’s and Children’s NHS Foundation Trust, Birmingham, UK PubMed articlesGoogle scholar articles
  • Andrew K Ewer Neonatal Unit, Birmingham Women’s and Children’s NHS Foundation Trust, Birmingham, UK Institute of Metabolism and Systems Research, University of Birmingham, Birmingham, UK PubMed articlesGoogle scholar articles
  • Mark D Kilby West Midlands Fetal Medicine Centre, Birmingham Women’s and Children’s NHS Foundation Trust, Birmingham, UK Institute of Metabolism and Systems Research, University of Birmingham, Birmingham, UK PubMed articlesGoogle scholar articles
  1. Correspondence to Professor Mark D Kilby, West Midlands Fetal Medicine Centre, Birmingham Women’s and Children’s NHS Foundation Trust, Birmingham B15 2TG, UK; m.d.kilby{at}bham.ac.uk
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Citation

Mone F, Quinlan-Jones E, Ewer AK, et al
Exome sequencing in the assessment of congenital malformations in the fetus and neonate
Archives of Disease in Childhood - Fetal and Neonatal Edition 2019;104:F452-F456.

Publication history

  • Received October 8, 2018
  • Revised December 31, 2018
  • Accepted January 2, 2019
  • First published February 1, 2019.
Online issue publication 
June 19, 2019

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© Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ.