Detection of Clinically Relevant Monogenic Copy-Number Variants by a Comprehensive Genome-Wide Microarray with Exonic Coverage.
Chau MHK, Anderson SA, Song R, Cooper L, Ward PA, Yuan B, Shaw C, Stankiewicz P, Cheung SW, Vossaert L, Wang Y, Owen NM, Smith J, Bacino CA, Schulze KV, Bi W.
Chau MHK, et al. Among authors: cooper l.
Clin Chem. 2025 Jan 3;71(1):141-154. doi: 10.1093/clinchem/hvae188.
Clin Chem. 2025.
PMID: 39749505