Prenatal chromosomal microarray testing of fetuses with ultrasound structural anomalies: A prospective cohort study of over 1000 consecutive cases-Reference-Cited by-同舟云学术

Prenatal chromosomal microarray testing of fetuses with ultrasound structural anomalies: A prospective cohort study of over 1000 consecutive cases

Published:2019-08-22 Issue:12 Volume:39 Page:1064-1069
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenatal Diagnosis

Author:

Chong Hsu P.¹,Hamilton Susan²,Mone Fionnuala¹²^ORCID,Cheung Ka Wang³^ORCID,Togneri Fiona S.²,Morris Rachel K.¹⁴^ORCID,Quinlan‐Jones Elizabeth¹⁴,Williams Denise²,Allen Stephanie²,McMullan Dominic J.²,Kilby Mark D.¹⁴^ORCID

Affiliation:

1. Fetal Medicine CentreBirmingham Women's and Children's NHS Foundation Trust Birmingham UK

2. West Midlands Regional Genetics Laboratory and Clinical Genetics ServiceWomen's and Children's NHS Foundation Trust Birmingham UK

3. Department of Obstetrics and GynaecologyQueen Mary Hospital, The University of Hong Kong Hong Kong

4. Institute of Metabolism and Systems ResearchUniversity of Birmingham Birmingham UK

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pd.5545

Reference24 articles.

1. Prenatal diagnosis by chromosomal microarray analysis

2. MoneF Quinlan‐JonesE EwerAK KilbyMD.Exome sequencing in the assessment of congenital malformations in the fetus and neonate. Arch Dis Child Fetal Neonatal Ed.2019Feb 1. pii: fetalneonatal‐2018‐316352. doi:https://doi.org/10.1136/archdischild‐2018‐316352. [Epub ahead of print]

3. Estimating Global Burden of Disease due to congenital anomaly: an analysis of European data

4. First‐trimester contingent screening for trisomies 21, 18 and 13 by fetal nuchal translucency and ductus venosus flow and maternal blood cell‐free DNA testing

5. Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data

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