Genome sequencing with gene panel-based analysis for rare inherited conditions in a publicly funded healthcare system: implications for future testing. (2023)
Attributed to:
The Scottish Genomes Partnership
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1038/s41431-022-01226-3
PubMed Identifier: 36474026
Publication URI: http://europepmc.org/abstract/MED/36474026
Type: Journal Article/Review
Volume: 31
Parent Publication: European journal of human genetics : EJHG
Issue: 2
ISSN: 1018-4813