Article

Genetic Architecture of CHD in NICU patients – UMC Ljubljana Experience

2024-05-13

Abstract excerpt

Congenital heart disease (CHD) is the most commonly detected congenital anomaly and affects up to 1 % of all live-born neonates. Current guidelines support the use of Chromosomal Microarray Analysis (CMA) and Next Generation Sequencing (NGS) as diagnostic approaches to identify genetic causes. The aim of our study was to evaluate the diagnostic yield of CMA and NGS in a cohort of neonates with both isolated and sy...

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Literature Corpus work: 4873c306-d773-5f10-bb5a-b5f7213869ea
DOI: 10.20944/preprints202405.0840.v1

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