Purpose The present study aims to evaluate the utility of high-resolution single-nucleotide
polymorphism (SNP) arrays in fetuses with ventricular septal defects (VSDs) with or without …

Objectives To evaluate the usefulness of chromosomal microarray analysis in fetuses with
ventricular septal defects (VSDs) with or without associated anomalies and normal …

Background This study aimed to evaluate the applicability of chromosomal microarray
analysis (CMA), rather than traditional chromosome analysis, in prenatal diagnosis of …

Objective This study aimed to detect genomic imbalances in fetuses with congenital heart
defect (CHD) by high‐resolution single‐nucleotide polymorphism (SNP) array. Methods A …

Introduction Ventricular septal defect (VSD) represents the most common type of congenital
cardiac anomaly, affecting more than 1 in 300 live births. The objective of this study was to …

Objective: In the study, we investigated the genetic etiology of the ventricular septal defect
(VSD) and comprehensively evaluated the diagnosis rate of prenatal chromosomal …

Objectives: To explore chromosomal variations, including copy number variations (CNVs), in
fetuses with conotruncal heart defect (CTD). Methods: During a 5-year period, a total of 129 …

Objectives: To evaluate the usefulness of single-nucleotide polymorphism (SNP) array for
prenatal genetic diagnosis of congenital heart defect (CHD), we used this approach to detect …

Objective To evaluate the association between prenatally detected isolated ventricular
septum defects (VSDs) and chromosomal aberrations in a nationwide study in Denmark …

Objective To evaluate the utility of chromosomal microarray analysis (CMA) in fetuses with
isolated ventricular septal defect (VSD) and to explore the favorable factors for predicting …