MHK, C., SA, A., R, S., L, C., PA, W., B, Y., . . . W, B. (2025). Detection of Clinically Relevant Monogenic Copy-Number Variants by a Comprehensive Genome-Wide Microarray with Exonic Coverage. Clinical chemistry, 71(1), 141. https://doi.org/10.1093/clinchem/hvae188
Chicago Style (17th ed.) CitationMHK, Chau, et al. "Detection of Clinically Relevant Monogenic Copy-Number Variants by a Comprehensive Genome-Wide Microarray with Exonic Coverage." Clinical Chemistry 71, no. 1 (2025): 141. https://doi.org/10.1093/clinchem/hvae188.
MLA (9th ed.) CitationMHK, Chau, et al. "Detection of Clinically Relevant Monogenic Copy-Number Variants by a Comprehensive Genome-Wide Microarray with Exonic Coverage." Clinical Chemistry, vol. 71, no. 1, 2025, p. 141, https://doi.org/10.1093/clinchem/hvae188.