APA   Click to copy
Paschal, C., Beck, A., Gillentine, M., Narayanan, J., Reed, P., Galey, M., & Miller, D. (2023). O33: Concordance of long-read genome sequencing with methylation calling with clinical testing for individuals with Prader-Willi or Angelman Syndrome. Genetics in Medicine Open, 1, 100459. https://doi.org/10.1016/j.gimo.2023.100459

Chicago/Turabian   Click to copy
Paschal, Cate, Anita Beck, Madelyn Gillentine, Jaya Narayanan, Paxton Reed, Miranda Galey, and Danny Miller. “O33: Concordance of Long-Read Genome Sequencing with Methylation Calling with Clinical Testing for Individuals with Prader-Willi or Angelman Syndrome.” Genetics in Medicine Open 1 (2023): 100459.

MLA   Click to copy
Paschal, Cate, et al. “O33: Concordance of Long-Read Genome Sequencing with Methylation Calling with Clinical Testing for Individuals with Prader-Willi or Angelman Syndrome.” Genetics in Medicine Open, vol. 1, Elsevier {BV}, 2023, p. 100459, doi:10.1016/j.gimo.2023.100459.

@article{paschal2023a,
  title = {O33: Concordance of long-read genome sequencing with methylation calling with clinical testing for individuals with Prader-Willi or Angelman Syndrome},
  year = {2023},
  journal = {Genetics in Medicine Open},
  pages = {100459},
  publisher = {Elsevier {BV}},
  volume = {1},
  doi = {10.1016/j.gimo.2023.100459},
  author = {Paschal, Cate and Beck, Anita and Gillentine, Madelyn and Narayanan, Jaya and Reed, Paxton and Galey, Miranda and Miller, Danny}
}