@misc{indiciaefd4fc916caed,
  title = {Multi-omics profiling reveals MAGEL2-driven defects in human corticogenesis shared across Prader-Willi and Schaaf-Yang syndromes.},
  author = {Buecking, J. and Güler, B. E. and Eibl, M. and Ali, A. S. and Walczuch, T. and Beschauner, T. and Theiss, S. and Spanjaard, M. and Hinderhofer, K. and Herrmann-Sim, F. and de Esch, C. E. and Tai, D. J. C. and Talkowski, M. E. and Krijgsveld, J. and Schaaf, C. P. and Laugsch, M.},
  year = {2026},
  doi = {10.64898/2026.05.01.722223},
  url = {https://www.biorxiv.org/content/10.64898/2026.05.01.722223v1},
  note = {Source identifier: 10.64898/2026.05.01.722223}
}