A yeast model for the study of human DFNA5, a gene mutated in nonsyndromic hearing impairment. by Gregan, J, Van Laer, L, Lieto, L, Van Camp, G, Kearsey, S

Homozygous SMAD6 variants in two unrelated patients with craniosynostosis and radioulnar synostosis by Luyckx, I, Walton, IS, Boeckx, N, Van Schil, K, Pang, C, De Praeter, M, Lord, H, Watson, CM, Bonthron, DT, Van Laer, L, Wilkie, AOM, Loeys, B

Whole Exome Sequencing is a Sensitive and Cost-Effective Means of Detecting Mutations in Patients with Marfan Syndrome and Osteogenesis Imperfecta by Duncan, E, McInerney-Leo, A, Leo, P, Gardiner, B, Marshall, M, Coucke, P, Loeys, B, West, M, West, J, Wordsworth, P, Zankl, A, Brown, M, van Laer, L