Use of genome sequencing to hunt for cryptic second-hit variants: analysis of 31 cases recruited to the 100 000 Genomes Project. (2023)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1136/jmg-2023-109362
PubMed Identifier: 37558402
Publication URI: http://europepmc.org/abstract/MED/37558402
Type: Journal Article/Review
Volume: 60
Parent Publication: Journal of medical genetics
Issue: 12
ISSN: 0022-2593