GENETIC ABNORMALITIES IDENTIFIED BY CHROMOSOMAL MICROARRAY IN NEONATES WITH CONGENITAL HEART DISEASE
2019
Over the past two decades, there has been a notable expansion in the field of genetic testing. A previous study from our institution reports the incidence of genetic abnormalities detected in neonates with congenital heart disease (CHD) by karyotyping and fluorescence in situ hybridization (FISH).
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