APA   Click to copy
Miller, D. E., Galey, M., Fletcher, S. N., Lannert, K., Wheeler, M. M., Kandhaya-Pillai, R., … Johnsen, J. M. (2022). Long-Read Sequencing Resolves Complex Structural Variants and Identifies Missing Disease-Causing Variants in Unsolved Cases of Hemophilia. Blood, 140, 10716–10717. https://doi.org/10.1182/blood-2022-169355

Chicago/Turabian   Click to copy
Miller, Danny E., Miranda Galey, Shelley N Fletcher, Kerry Lannert, Marsha M Wheeler, Renuka Kandhaya-Pillai, Junko Oshima, Barbara A. Konkle, Evan E Eichler, and Jill M. Johnsen. “Long-Read Sequencing Resolves Complex Structural Variants and Identifies Missing Disease-Causing Variants in Unsolved Cases of Hemophilia.” Blood 140 (November 2022): 10716–10717.

MLA   Click to copy
Miller, Danny E., et al. “Long-Read Sequencing Resolves Complex Structural Variants and Identifies Missing Disease-Causing Variants in Unsolved Cases of Hemophilia.” Blood, vol. 140, American Society of Hematology, Nov. 2022, pp. 10716–17, doi:10.1182/blood-2022-169355.

@article{miller2022a,
  title = {Long-Read Sequencing Resolves Complex Structural Variants and Identifies Missing Disease-Causing Variants in Unsolved Cases of Hemophilia},
  year = {2022},
  month = nov,
  journal = {Blood},
  pages = {10716--10717},
  publisher = {American Society of Hematology},
  volume = {140},
  doi = {10.1182/blood-2022-169355},
  author = {Miller, Danny E. and Galey, Miranda and Fletcher, Shelley N and Lannert, Kerry and Wheeler, Marsha M and Kandhaya-Pillai, Renuka and Oshima, Junko and Konkle, Barbara A. and Eichler, Evan E and Johnsen, Jill M.},
  month_numeric = {11}
}