Genomic testing and molecular diagnosis among infants with congenital heart disease in the neonatal intensive care unit.
Erica E D'SouzaTina O FindleyRachel HuZahra S H KhazalRachel SignorelloCamille DashAlissa M D'GamaHenry A FeldmanPankaj B AgrawalMonica Hsiung WojcikSarah U MortonPublished in: Journal of perinatology : official journal of the California Perinatal Association (2024)
Infants with suspicion of a genetic disorder with CHD had similar rates of molecular diagnosis as those without CHD. These results support a role for genetic testing among NICU infants with CHD.
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