Increased prenatal detection of 22q11.2 deletion and 22q11.2 duplication after introduction of nationwide prenatal screening for trisomy 21, trisomy 13, and trisomy 18

Author:

Steffensen Ellen Hollands12ORCID,Hyett Jonathan23,Petersen Olav Bjørn45,Vogel Ida12,

Affiliation:

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

2. Center for Fetal Diagnostics, Department of Clinical Medicine Aarhus University Aarhus N Denmark

3. Royal Prince Alfred Hospital, Women and Babies Sydney Institute for Women, Children and their Families Sydney New South Wales Australia

4. Center of Fetal Medicine and Pregnancy, Department of Obstetrics Copenhagen University Hospital København Ø Denmark

5. Department of Clinical Medicine University of Copenhagen København N Denmark

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference31 articles.

1. National screening guidelines and developments in prenatal diagnoses and live births of Down syndrome in 1973-2016 in Denmark

2. Impact of a new national screening policy for Down's syndrome in Denmark: population based cohort study;Ekelund CK;BMJ,2008

3. Sundhedsstyrelsen.Retningslinjer for fosterdiagnostik: prænatal information risikovurdering rådgivning og diagnostik. Version 1.0. Sundhedsstyrelsen; 2004.

4. The Danish Fetal Medicine Database: Annual Reports 2012‐2016.https://www.dfms.dk/new-page-33. The Danish Fetal Medicine Research Group.

5. Contingent first-trimester screening for aneuploidies with cell-free DNA in a Danish clinical setting

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