@misc{indiciaefb9e298fe9a5,
  title = {Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome},
  author = {Alharatani, R. and Vervari, A. and Beleza-Meireles, A. and Ji, W. and Mis, E. and Patterson, Q. and Griffin, J. and Bhujel, N. and Chang, C. and Dixit, A. and Konstantino, M. and Healy, C. and Hannan, S. and Neo, N. and Cash, A. and Li, D. and Bhoj, E. and Zackai, E. and Cleaver, R. and Baralle, D. and McEntagart, M. and Newbury-Ecob, R. and Scott, R. and Hurst, J. and Au, P. Y. B. and Hosey, M. T. and Marciano, D. and Khokha, M. and Lakhani, S. and Liu, K.},
  year = {2019},
  doi = {10.1101/711184},
  url = {https://www.biorxiv.org/content/10.1101/711184v1},
  note = {Source identifier: 10.1101/711184}
}