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APA Citation
Watson, C. M., Holliday, D. L., Crinnion, L. A., & Bonthron, D. T. (2022). long‐read nanopore DNA sequencing can resolve complex intragenic duplication/deletion variants, providing information to enable preimplantation genetic diagnosis. Prenatal diagnosis, 42, 226–232. http://access.bl.uk/ark:/81055/vdc_100151264278.0x000059