Noninvasive prenatal testing for 22q11.2 deletion syndrome: deeper sequencing increases the positive predictive value
- PMID: 25986033
- DOI: 10.1016/j.ajog.2015.05.028
Noninvasive prenatal testing for 22q11.2 deletion syndrome: deeper sequencing increases the positive predictive value
Comment on
-
Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes.Am J Obstet Gynecol. 2015 Mar;212(3):332.e1-9. doi: 10.1016/j.ajog.2014.11.041. Epub 2014 Dec 2. Am J Obstet Gynecol. 2015. PMID: 25479548
Similar articles
-
Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes.Am J Obstet Gynecol. 2015 Mar;212(3):332.e1-9. doi: 10.1016/j.ajog.2014.11.041. Epub 2014 Dec 2. Am J Obstet Gynecol. 2015. PMID: 25479548
-
Detection of chromosome abnormalities using current noninvasive prenatal testing: A multi-center comparative study.Biosci Trends. 2018 Jul 17;12(3):317-324. doi: 10.5582/bst.2018.01044. Epub 2018 Jun 28. Biosci Trends. 2018. PMID: 29952350
-
Clinical experience with single-nucleotide polymorphism-based non-invasive prenatal screening for 22q11.2 deletion syndrome.Ultrasound Obstet Gynecol. 2016 Feb;47(2):177-83. doi: 10.1002/uog.15754. Epub 2016 Jan 5. Ultrasound Obstet Gynecol. 2016. PMID: 26396068 Free PMC article.
-
Cell-Free DNA Screening for Aneuploidy and Microdeletion Syndromes.Obstet Gynecol Clin North Am. 2018 Mar;45(1):13-26. doi: 10.1016/j.ogc.2017.10.001. Obstet Gynecol Clin North Am. 2018. PMID: 29428281 Review.
-
Introducing WISECONDOR for noninvasive prenatal diagnostics.Expert Rev Mol Diagn. 2014 Jun;14(5):513-5. doi: 10.1586/14737159.2014.919855. Epub 2014 May 16. Expert Rev Mol Diagn. 2014. PMID: 24831532 Review.
Cited by
-
Performance of whole-genome promoter nucleosome profiling of maternal plasma cell-free DNA for prenatal noninvasive prediction of fetal macrosomia: a retrospective nested case-control study in mainland China.BMC Pregnancy Childbirth. 2022 Sep 10;22(1):698. doi: 10.1186/s12884-022-05027-w. BMC Pregnancy Childbirth. 2022. PMID: 36088304 Free PMC article.
-
Comprehensive Evaluation of Non-invasive Prenatal Screening to Detect Fetal Copy Number Variations.Front Genet. 2021 Jul 16;12:665589. doi: 10.3389/fgene.2021.665589. eCollection 2021. Front Genet. 2021. PMID: 34335682 Free PMC article.
-
Prenatal Screening for 22q11.2 Deletion Using a Targeted Microarray-Based Cell-Free DNA Test.Fetal Diagn Ther. 2018;44(4):299-304. doi: 10.1159/000484317. Epub 2017 Nov 8. Fetal Diagn Ther. 2018. PMID: 29131052 Free PMC article.
-
Recent advances in prenatal genetic screening and testing.F1000Res. 2016 Oct 28;5:2591. doi: 10.12688/f1000research.9215.1. eCollection 2016. F1000Res. 2016. PMID: 27853526 Free PMC article. Review.
-
Noninvasive prenatal screening for fetal aneuploidy, 2016 update: a position statement of the American College of Medical Genetics and Genomics.Genet Med. 2016 Oct;18(10):1056-65. doi: 10.1038/gim.2016.97. Epub 2016 Jul 28. Genet Med. 2016. PMID: 27467454
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical
