Validation of a SNP-based non-invasive prenatal test to detect the fetal 22q11.2 deletion in maternal plasma samples
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference23 articles.
1. Presence of fetal DNA in maternal plasma and serum;YM Lo;Lancet,1997
2. Noninvasive prenatal testing: the paradigm is shifting rapidly;LS Chitty;Prenatal diagnosis,2013
3. Clinical outcome of subchromosomal events detected by whole-genome noninvasive prenatal testing;J Helgeson;Prenatal diagnosis,2015
4. Clinical experience with single-nucleotide polymorphism-based non-invasive prenatal screening for 22q11.2 deletion syndrome;SJ Gross;Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology,2016
5. Clinical validation of a noninvasive prenatal test for genomewide detection of fetal copy number variants;RB Lefkowitz;American journal of obstetrics and gynecology,2016
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1. Rapid and accurate genotype imputation from low coverage short read, long read, and cell free DNA sequence;2024-07-22
2. 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
3. Prenatal vs postnatal diagnosis of 22q11.2 deletion syndrome: cardiac and noncardiac outcomes through 1 year of age;American Journal of Obstetrics and Gynecology;2023-09
4. Detection of 22q11.2 deletion syndrome by single-nucleotide polymorphism based non-invasive prenatal test;Indian Journal of Obstetrics and Gynecology Research;2023-08-15
5. Chromosome 22q11.2 Deletion (DiGeorge Syndrome): Immunologic Features, Diagnosis, and Management;Current Allergy and Asthma Reports;2023-03-10
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