Noninvasive prenatal testing for fetal trisomy in mixed risk factors pregnancy population
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynecology
Reference8 articles.
1. Prenatal diagnosis of de novo interstitial deletions involving 5q23.1-q23.3 and 18q12.1-q12.3 by array CGH using uncultured amniocytes in a pregnancy with fetal interrupted aortic arch and atrial septal defect;Chen;Gene,2013
2. Is it possible to use cell-free fetal DNA to perform prenatal tests for multiple pregnancies?;Li;Taiwan J Obstet Gynecol,2014
3. Noninvasive prenatal testing for fetal trisomy in mixed risk factors pregnancy population;Li;Taiwan J Obstet Gynecol,2015
4. Screening for trisomies in circulating DNA;Greene;New Eng J Med,2014
5. Introducing the noninvasive prenatal test for trisomy 21 in Belgium: a cost-consequences analysis;Neyt;BMJ Open,2014
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2. Conservative surgical treatment of adenomyosis to improve fertility: Controversial values, indications, complications, and pregnancy outcomes;Taiwanese Journal of Obstetrics and Gynecology;2015-12
3. Outstanding research paper awards of the 2014 Taiwanese Journal of Obstetrics and Gynecology;Taiwanese Journal of Obstetrics and Gynecology;2015-06
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