Cell-free DNA screening for prenatal detection of 22q11.2 deletion syndrome
Author:
Funder
Eunice Kennedy Shriver National Institute of Child Health and Human Development
Publisher
Elsevier BV
Subject
Obstetrics and Gynecology
Reference33 articles.
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2. Analysis of cell-free DNA in maternal blood in screening for aneuploidies: updated meta-analysis;Gil;Ultrasound Obstet Gynecol,2017
3. Cell-free DNA analysis for noninvasive examination of trisomy;Norton;N Engl J Med,2015
4. Clinical experience and follow-up with large scale single-nucleotide polymorphism-based noninvasive prenatal aneuploidy testing;Dar;Am J Obstet Gynecol,2014
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1. Prospective prenatal cell-free DNA screening for genetic conditions of heterogenous etiologies;Nature Medicine;2024-01-22
2. Decoding 22q11.2: prenatal profiling and first‐trimester risk assessment in Danish nationwide cohort;Ultrasound in Obstetrics & Gynecology;2024-01
3. Impact of high‐risk prenatal screening results for 22q11.2 deletion syndrome on obstetric and neonatal management: Secondary analysis from the SMART study;Prenatal Diagnosis;2023-12
4. A Diagnosis of Maternal 22q Duplication and Mosaic Deletion following Prenatal Cell-Free DNA Screening;Case Reports in Genetics;2023-11-20
5. 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
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