The Use of Chromosomal Microarray Analysis in Prenatal Diagnosis
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynaecology
Reference38 articles.
1. Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies;Miller;Am J Hum Genet,2010
2. Detection of pathogenic gene copy number variations in patients with mental retardation by genomewide oligonucleotide array comparative genomic hybridization;Fan;Hum Mutat,2007
3. Committee opinion No. 581: the use of chromosomal microarray analysis in prenatal diagnosis;Obstet Gynecol,2013
4. ACOG Practice Bulletin No. 88, December 2007. Invasive prenatal testing for aneuploidy;American College of Obstetricians and Gynecologists;Obstet Gynecol,2007
5. Practice Bulletin No. 162: prenatal diagnostic testing for genetic disorders;Obstet Gynecol,2016
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1. Prenatal diagnosis and molecular cytogenetic characterization of fetuses with central nervous system anomalies using chromosomal microarray analysis: a seven-year single-center retrospective study;Scientific Reports;2024-01-27
2. Clinical Experience of Prenatal Chromosomal Microarray Analysis in 6159 Ultrasonically Abnormal Fetuses;Reproductive Sciences;2023-11-27
3. Overview of genetic testing in Prader-Willi syndrome;Expert Opinion on Orphan Drugs;2023-09-28
4. Invasive prenatal diagnosis in the era of cell-free fetal DNA: experience at a single center;Minerva Obstetrics and Gynecology;2023-09
5. Diagnostic Yield of Exome Sequencing in Prenatal Agenesis of Corpus Callosum: A Systematic Review and Meta‐analysis;Ultrasound in Obstetrics & Gynecology;2023-07-31
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