Chromosomal microarray as primary diagnostic genomic tool for pregnancies at increased risk within a population-based combined first-trimester screening program-Reference-Cited by-同舟云学术

Chromosomal microarray as primary diagnostic genomic tool for pregnancies at increased risk within a population-based combined first-trimester screening program

Published:2018-03-04 Issue:4 Volume:51 Page:480-486
ISSN:0960-7692
Container-title:Ultrasound in Obstetrics & Gynecology
language:en
Short-container-title:Ultrasound Obstet Gynecol

Author:

Vogel I.¹²³^ORCID,Petersen O. B.²⁴,Christensen R.¹³,Hyett J.⁵,Lou S.²⁶,Vestergaard E. M.¹²³

Affiliation:

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

2. Center for Prenatal Diagnostics; Aarhus University Hospital; Aarhus Denmark

3. Institute of Biomedicine; Aarhus University Hospital; Aarhus Denmark

4. Department of Obstetrics and Gynecology; Aarhus University Hospital; Aarhus Denmark

5. Discipline of Obstetrics, Gynaecology and Neonatology; University of Sydney; Sydney Australia

6. DEFACTUM; Central Denmark Region; Denmark

Funder

Sundhed og Sygdom, Det Frie Forskningsråd

Novo Nordic Foundation

Publisher

Wiley

Subject

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

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/uog.17548/fullpdf

Reference32 articles.

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2. The Danish Fetal Medicine database;Ekelund;Clin Epidemiol,2016

3. Ten years of experience with first-trimester screening for fetal aneuploidy employing biochemistry from gestational weeks 6+0 to 13+6;Torring;Fetal Diagn Ther,2015

4. Prenatal diagnosis: array comparative genomic hybridization in fetuses with abnormal sonographic findings;Vestergaard;Acta Obstet Gynecol Scand,2013

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