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A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases. (2022)

First Author: Kingsmore SF

Attributed to: UK Biobank (core renewal) funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2022.08.003

PubMed Identifier: 36007526

Publication URI: http://europepmc.org/abstract/MED/36007526

Type: Journal Article/Review

Volume: 109

Parent Publication: American journal of human genetics

Issue: 9

ISSN: 0002-9297