Bonnard, C. Et Al. 2018. Novel mutations in the ciliopathy-associated gene CPLANE1 (C5orf42) cause OFD syndrome type VI rather than Joubert syndrome. EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.61, no.10 , 585-595.

Bonnard, C., Shbourl, M., Tonekaboni, S. H., Ng, A. Y. J., Tohari, S., Ghosh, K., ... Lai, A.(2018). Novel mutations in the ciliopathy-associated gene CPLANE1 (C5orf42) cause OFD syndrome type VI rather than Joubert syndrome. EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.61, no.10, 585-595.

Bonnard, Carine Et Al. "Novel mutations in the ciliopathy-associated gene CPLANE1 (C5orf42) cause OFD syndrome type VI rather than Joubert syndrome," EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.61, no.10, 585-595, 2018

Bonnard, Carine Et Al. "Novel mutations in the ciliopathy-associated gene CPLANE1 (C5orf42) cause OFD syndrome type VI rather than Joubert syndrome." EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.61, no.10, pp.585-595, 2018

Bonnard, C. Et Al. (2018) . "Novel mutations in the ciliopathy-associated gene CPLANE1 (C5orf42) cause OFD syndrome type VI rather than Joubert syndrome." EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.61, no.10, pp.585-595.

@article{article, author={Carine Bonnard Et Al. }, title={Novel mutations in the ciliopathy-associated gene CPLANE1 (C5orf42) cause OFD syndrome type VI rather than Joubert syndrome}, journal={EUROPEAN JOURNAL OF MEDICAL GENETICS}, year=2018, pages={585-595} }