@misc{indiciaef71f405b232d,
  title = {ASXL1 mutations that cause Bohring Opitz Syndrome (BOS) or acute myeloid leukemia share epigenomic and transcriptomic signatures},
  author = {Lin, I. and Awamleh, Z. and Wei, A. and Russell, B. and Weksberg, R. A. and Arboleda, V. A.},
  year = {2022},
  doi = {10.1101/2022.12.15.519823},
  url = {https://www.biorxiv.org/content/10.1101/2022.12.15.519823v1},
  note = {Source identifier: 10.1101/2022.12.15.519823}
}