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