Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease

Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease

Abstract Congenital heart disease (CHD) is the most common congenital anomaly and a major cause of infant morbidity and mortality. While morbidity and mortality are highest in infants with underlying genetic conditions, molecular diagnoses are ascertained in only ~20% of cases using widely adopted g...

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Bibliographic Details
Main Authors: Nathaly M. Sweeney, Shareef A. Nahas, Sh. Chowdhury, Sergey Batalov, Michelle Clark, Sara Caylor, Julie Cakici, John J. Nigro, Yan Ding, Narayanan Veeraraghavan, Charlotte Hobbs, David Dimmock, Stephen F. Kingsmore
Format: Article
Language:English
Published: Nature Publishing Group 2021-04-01
Series:npj Genomic Medicine
Online Access:https://doi.org/10.1038/s41525-021-00192-x

Internet

https://doi.org/10.1038/s41525-021-00192-x

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