Kievit, A. ., Tessadori, F. ., Douben, H. ., Jordens, I. ., Maurice, M. ., Hoogeboom, J. ., … van Haaften, G. . (2018). Variants in members of the cadherin-catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome. European Journal of Human Genetics : EJHG. https://doi.org/10.1038/s41431-017-0010-5 (Original work published 2018)

Leiter, S. ., Parker, V. ., Welters, A. ., Knox, R. ., Rocha, N. ., Clark, G. ., … Semple, R. . (2017). Hypoinsulinaemic, hypoketotic hypoglycaemia due to mosaic genetic activation of PI3-kinase. European Journal of Endocrinology, 177(2), 175-186. https://doi.org/10.1530/EJE-17-0132