Background: Congenital heart disease (CHD) is one of the most common birth defects;
however, the mechanisms underlying its development are poorly understood. Recently …

Objectives This study aimed to determine chromosomal abnormalities and copy number
variations (CNVs) in fetuses with congenital heart disease (CHD) by chromosomal …

Objective This study aimed to examine the effectiveness of the SNP array for the prenatal
diagnosis of congenital heart disease (CHD) screened by echocardiography. Patients and …

Congenital heart defects (CHD) are the most common congenital problems in neonates. The
basis for CHD is multifactorial, involving genetic and environmental components. The …

While the majority of patients have isolated heart disease, congenital heart disease (CHD)
may be associated with other congenital anomalies or syndromes. Our institution utilizes …

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 …

The prenatal diagnosis of congenital heart disease (CHD) is important because of mortality
risk. The onset of CHD varies, and depending on the malformation type, the risk of …

Purpose The aim of this meta-analysis was to evaluate the risk of chromosomal
abnormalities in fetuses with congenital heart disease (CHD). Methods Four literature …

Congenital heart disease (CHD) is the most common congenital anomaly and is an
important cause of infant morbidity and mortality. Besides the epigenetic and environmental …

Objective To evaluate comprehensively, using chromosomal microarray analysis (CMA) and
exome sequencing (ES), the prevalence of chromosomal abnormalities and sequence …