Our understanding of the genetics of congenital heart disease (CHD) is rapidly expanding;
however, many questions, particularly those relating to sporadic forms of disease, remain …

This 8th Edition of Moss and Adams' Heart Disease in Infants, Children, and Adolescents:
Including the Fetus and Young Adult, provides updated and useful information from leading …

Background There is no consensus on the effectiveness of prenatal diagnosis except for
hospitalized outcomes. Hence, a meta-analysis of published literature was conducted to …

Congenital heart disease (CHD) is the most common class of major malformations in
humans. The historical association with large chromosomal abnormalities foreshadowed the …

Objective To investigate the prevalence of extracardiac anomalies (ECA) in prenatally
diagnosed congenital heart diseases (CHD), and to provide more information for counseling …

Background Congenital heart disease (CHD) is often associated with extracardiac
malformations (ECMs) and genetic syndromes. Aims To determine the effect of cytogenetic …

Despite the extensive information available on the different genetic, epigenetic, and
molecular features of cardiogenesis, the origin of congenital heart defects remains unknown …

Recent advances in understanding the genetic causes and anatomic subtypes of cardiac
defects have revealed new links between genetic etiology, pathogenetic mechanisms and …

Congenital heart defects (CHD) are malformations present at birth that occur during heart
development. Increasing evidence supports a genetic origin of CHD, but in the process …

Nuclear-enriched abundant transcript 1 (NEAT1), a vital long noncoding RNA (lncRNA),
exhibits the functions in disparate cancers. Nevertheless, the influences of NEAT1 in …