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Published in 2021 at "Diagnostics"
DOI: 10.3390/diagnostics11020337
Abstract: Chromosomal microarray analysis (CMA), recently introduced following conventional cytogenetic technology, can detect submicroscopic copy-number variations (CNVs) in cases previously diagnosed as “cytogenetically benign”. At present, rapid and accurate chromosomal analysis is required in prenatal diagnostics,…
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Keywords:
submicroscopic;
rapid screening;
submicroscopic cnvs;
new prenatal ... See more keywords