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Paper Details

Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease.
NPJ Genom Med
36
2021
CHD, Congenital heart disease, children, congenital anomaly, congenital heart disease, genetic conditions, genetic disease, genetic diseases, infant, infants, microarraygene panels, rWGS, structural CHD
Author NameAffiliation
Serge BatalovRady Children's Institute for Genomic Medicine
Michelle M ClarkRady Children's Institute for Genomic Medicine
Julie A CakiciRady Children's Institute for Genomic Medicine
Julie A CakiciUniversity of California San Diego
Ashok VeeraraghavanRady Children's Institute for Genomic Medicine
David DimmockRady Children's Institute for Genomic Medicine
Stephen F KingsmoreRady Children's Institute for Genomic Medicine
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