Rare novel variants in the ZIC3 gene cause X-linked heterotaxy

Aimee D. C. Paulussen, Anja Steyls, Jo Vanoevelen, Florence H. J. van Tienen, Ingrid P. C. Krapels, Godelieve R. F. Claes, Sonja Chocron, Crool Velter, Gita M. Tan-Sindhunata, Catarina Lundin, Irene Valenzuela, Balint Nagy, Iben Bache, Lisa Leth Maroun, Kristiina Avela, Han G. Brunner, Hubert J. M. Smeets, Jeroen Bakkers, Arthur van den Wijngaard

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Pages (from-to)1783-1791
JournalEuropean Journal of Human Genetics
Volume24
Issue number12
DOIs
Publication statusPublished - Dec 2016

Cite this

Paulussen, A. D. C., Steyls, A., Vanoevelen, J., van Tienen, F. H. J., Krapels, I. P. C., Claes, G. R. F., ... van den Wijngaard, A. (2016). Rare novel variants in the ZIC3 gene cause X-linked heterotaxy. European Journal of Human Genetics, 24(12), 1783-1791. https://doi.org/10.1038/ejhg.2016.91