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Paper Details

A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases.
Am J Hum Genet
55
2022
NBS, childhood disorders, children, critically, critically ill, genetic disease, genetic diseases, genetic disorders, rWGS
Author NameAffiliation
Stephen F KingsmoreRady Children's Institute for Genomic Medicine, USA Rady Children's Hospital, USA Keck Graduate Institute
Serge BatalovRady Children's Institute for Genomic Medicine, USA Rady Children's Hospital
David DimmockRady Children's Institute for Genomic Medicine, USA Rady Children's Hospital
Annette FeigenbaumRady Children's Institute for Genomic Medicine, USA Rady Children's Hospital, University of California San Diego
Erwin FriseInc.
Robert C GreenBroad Institute, Ariadne Labs and Harvard Medical School
Martin G ReeseInc.
Ashok VeeraraghavanRady Children's Institute for Genomic Medicine, USA Rady Children's Hospital
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