Evidence review and considerations for use of first line genome sequencing to diagnose rare genetic disorders.
Wigby KM, Brockman D, Costain G, Hale C, Taylor SL, Belmont J, Bick D, Dimmock D, Fernbach S, Greally J, Jobanputra V, Kulkarni S, Spiteri E, Taft RJ.
Wigby KM, et al. Among authors: costain g.
NPJ Genom Med. 2024 Feb 26;9(1):15. doi: 10.1038/s41525-024-00396-x.
NPJ Genom Med. 2024.
PMID: 38409289
Free PMC article.
Review.