1. 2020
  2. The association of CTDP1 mutation with malformations of cortical development

    Yildirim, H., Kerkhove, L., Dimitrov, B., Cannaerts, E., Sermon, K., Stouffs, K. & Jansen, A., 6 Mar 2020.

    Research output: Unpublished contribution to conferencePoster

  3. 2019
  4. Novel pathogenic SMAD2 variants in five families with arterial aneurysm and dissection: Further delineation of the phenotype

    Cannaerts, E., Kempers, M., Maugeri, A., Marcelis, C., Gardeitchik, T., Richer, J., Micha, D., Beauchesne, L., Timmermans, J., Vermeersch, P., Meyten, N., Chénier, S., Van De Beek, G., Peeters, N., Alaerts, M., Schepers, D., Van Laer, L., Verstraeten, A. & Loeys, B., 1 Apr 2019, In : Journal of Medical Genetics. 56, 4, p. 220-227 8 p.

    Research output: Contribution to journalArticle

ID: 40416591