Robertson, E., Grinton, B., Oliver, K., Fearnley, L., Hildebrand, M., Sadleir, L., . . . Bahlo, M. (2025). Identifying individuals with rare disease variants by inferring shared ancestral haplotypes from SNP array data. NAR genomics and bioinformatics, 7(2), lqaf033. https://doi.org/10.1093/nargab/lqaf033
Chicago Style (17th ed.) CitationRobertson, Erandee, et al. "Identifying Individuals with Rare Disease Variants by Inferring Shared Ancestral Haplotypes from SNP Array Data." NAR Genomics and Bioinformatics 7, no. 2 (2025): lqaf033. https://doi.org/10.1093/nargab/lqaf033.
MLA (9th ed.) CitationRobertson, Erandee, et al. "Identifying Individuals with Rare Disease Variants by Inferring Shared Ancestral Haplotypes from SNP Array Data." NAR Genomics and Bioinformatics, vol. 7, no. 2, 2025, p. lqaf033, https://doi.org/10.1093/nargab/lqaf033.