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Genome sequencing with gene panel-based analysis for rare inherited conditions in a publicly funded healthcare system: implications for future testing. (2023)

First Author: Hocking LJ

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