Performance of noninvasive prenatal screening for 22q11.2 deletion syndrome in the SMART study
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynecology
Reference3 articles.
1. Cell-free DNA screening for prenatal detection of 22q11.2 deletion syndrome;Dar;Am J Obstet Gynecol,2022
2. Estimate of the contemporary live-birth prevalence of recurrent 22q11.2 deletions: a cross-sectional analysis from population-based newborn screening;Blagojevic;CMAJ Open,2021
3. Cell-free DNA screening for trisomies 21, 18 and 13 in pregnancies at low and high risk for aneuploidy with genetic confirmation;Dar;Am J Obstet Gynecol,2022
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1. Antenatal reproductive screening for pregnant people including preconception: Provides the best reproductive opportunity for informed consent, quality, and safety;Best Practice & Research Clinical Obstetrics & Gynaecology;2024-09
2. Understanding the Variability of 22q11.2 Deletion Syndrome: The Role of Epigenetic Factors;Genes;2024-02-29
3. Perinatal Diagnosis and Management of a Case with Interrupted Aortic Arch, Pulmonary Valve Dysplasia and 22q11.2 Deletion: A Case Report;Medicina;2023-10-16
4. Clinical Course and Outcome of Prenatally Detected 22q11.2 Deletion Syndrome—A Retrospective Analysis;Diagnostics;2023-07-01
5. Chromosome 22q11.2 Deletion Syndrome: A Comprehensive Review of Molecular Genetics in the Context of Multidisciplinary Clinical Approach;International Journal of Molecular Sciences;2023-05-05
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