Nuchal translucency distributions for different chromosomal anomalies in a large unselected population cohort-Reference-Cited by-同舟云学术

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Nuchal translucency distributions for different chromosomal anomalies in a large unselected population cohort

Published:2015-11-19 Issue:1 Volume:36 Page:49-55
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat Diagn

Author:

Christiansen Marianne¹,Ekelund Charlotte K.²,Petersen Olav Bjørn¹,Hyett Jon³,Eastwood Nathan⁴,Ball Susan⁵,Tabor Ann²,Vogel Ida⁶

Affiliation:

1. Fetal Medicine Unit, Department of Obstetrics and Gynecology; Aarhus University Hospital; Aarhus Denmark

2. Center for Fetal Medicine, Department of Obstetrics; Copenhagen University Hospital Rigshospitalet; Copenhagen Denmark

3. Department of High Risk Obstetrics; Royal Prince Alfred Hospital; Sydney Australia

4. Centre for Biostatistics, Bioinformatics and Biomarkers; Plymouth University; Plymouth United Kingdom

5. NIHR CLAHRC South West Peninsula (PenCLAHRC); University of Exeter Medical School; Exeter United Kingdom

6. Department of Clinical Genetics; Aarhus University Hospital; Aarhus Denmark

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Reference17 articles.

1. A mixture model of nuchal translucency thickness in screening for chromosomal defects;Wright;Ultrasound Obstet Gynecol,2008

2. Relation between increased fetal nuchal translucency thickness and chromosomal defects;Kagan;Obstet Gynecol,2006

3. Screening for trisomies 21, 18 and 13 by maternal age, fetal nuchal translucency, fetal heart rate, free beta-hCG and pregnancy-associated plasma protein-A;Kagan;Hum Reprod,2008

4. Potential diagnostic consequences of applying non-invasive prenatal testing: population-based study from a country with existing first-trimester screening;Petersen;Ultrasound Obstet Gynecol,2014

5. The Danish Fetal Medicine Database: Establishment, organization and quality assessment of the first trimester screening programme for trisomy 21 in Denmark 2008-2012;Ekelund;Acta Obstet Gynecol Scand,2015

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1. A Pain in the Neck: Lessons Learnt from Genetic Testing in Fetuses Detected with Nuchal Fluid Collections, Increased Nuchal Translucency versus Cystic Hygroma—Systematic Review of the Literature, Meta-Analysis and Case Series;Diagnostics;2022-12-23

2. Urinary Proteomics for Noninvasive Prenatal Screening of Trisomy 21: New Biomarker Candidates;OMICS: A Journal of Integrative Biology;2021-11-01

3. Screening for Fetal Aneuploidy and Sex Chromosomal Anomalies in a Pregnant Woman With Mosaicism for Turner Syndrome—Applications and Advantages of Cell-Based NIPT;Frontiers in Genetics;2021-09-14

4. The epidemiology of sex chromosome abnormalities;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2020-06

5. The utility of nuchal translucency ultrasound in identifying rare chromosomal abnormalities not detectable by cell‐free DNA screening;Prenatal Diagnosis;2019-12-02

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