Prenatal exome sequencing and impact on perinatal outcome: cohort study

Author:

Poljak B.1,Agarwal U.1ORCID,Alfirevic Z.12ORCID,Allen S.3,Canham N.4,Higgs J.4,Kaelin Agten A.1ORCID,Khalil A.56ORCID,Roberts D.1,Mone F.7ORCID,Navaratnam K.12ORCID

Affiliation:

1. Fetal Medicine Unit, Liverpool Women's Hospital NHS Foundation Trust Liverpool UK

2. Harris‐Wellbeing Research Centre University of Liverpool Liverpool UK

3. West Midlands Regional Genetics Laboratory and Clinical Genetics Service, Birmingham Women's and Children's NHS Foundation Trust Birmingham UK

4. Clinical Genetics Department Liverpool Women's Hospital NHS Foundation Trust Liverpool UK

5. Fetal Medicine Unit St George's University Hospitals NHS Foundation Trust, University of London London UK

6. Vascular Biology Research Centre Molecular and Clinical Sciences Research Institute, St George's University of London London UK

7. Centre for Public Health Queen's University Belfast Belfast UK

Publisher

Wiley

Subject

Obstetrics and Gynecology,Radiology, Nuclear Medicine and imaging,Reproductive Medicine,General Medicine,Radiological and Ultrasound Technology

Reference22 articles.

1. Exome sequencing in the assessment of congenital malformations in the fetus and neonate;Mone F;Arch Dis Child Fetal Neonatal Ed,2019

2. Public Health England.Fetal Anomaly Screening Programme (FASP): programme overview 2013.https://www.gov.uk/guidance/fetal‐anomaly‐screening‐programme‐overview[Accessed 23 June 2022].

3. His Majesty's Stationery Office (HMSO) UK.Abortion Act 1967(c. 87). HMSO: London UK 1967.

4. Royal College of Obstetricians and Gynaecologists.Termination of pregnancy for fetal abnormality in England Scotland and Wales: report of a working party 2010.https://rcog.org.uk/media/21lfvl0e/terminationpregnancyreport18may2010.pdf[Accessed 23 May 2022].

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