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 …

Abstract Objective Copy number variations (CNVs) detected by high-resolution single
nucleotide polymorphism microarrays (SNP arrays) have been associated with congenital …

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 …

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 …

Congenital heart defects (CHDs) are the most common birth defects in neonatal life. CHDs
could be presented as isolated defects or associated with developmental delay (DD) and/or …

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

Background With the increasing availability of chromosomal microarray analysis (CMA) for
congenital heart defect (CHD), genetic testing now faces new challenges due to results with …

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 …

Objectives To evaluate the usefulness of array‐based comparative genomic hybridization
(aCGH) for prenatal genetic diagnosis of congenital heart disease (CHD), with and without …

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