Abstract
Objectives
Chromosomal microarray analysis (CMA) allows genome-wide analysis to reveal unbalanced submicroscopic aberrations in prenatal diagnosis. However, the clinical impact of certain copy number variants (CNVs) remains difficult to assess prenatally. This study aims to evaluate the role of fetal ultrasound examination in the raising challenges for prenatal genetic counseling.
Chromosomal microarray analysis (CMA) allows genome-wide analysis to reveal unbalanced submicroscopic aberrations in prenatal diagnosis. However, the clinical impact of certain copy number variants (CNVs) remains difficult to assess prenatally. This study aims to evaluate the role of fetal ultrasound examination in the raising challenges for prenatal genetic counseling.
Original language | Undefined/Unknown |
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Pages (from-to) | S136-S137 |
Journal | Ultrasound in medicine & biology |
Volume | 43 |
DOIs | |
Publication status | Published - 2017 |