Whole exome sequencing identifies mutations in 10% of patients with familial non-syndromic cleft lip and/or palate in genes mutated in well-known syndromes

Basha, M., Demeer, B., Revencu, N., Helaers, R., Theys, S., Bou Saba, S., Boute, O., Devauchelle, B., Francois, G., Bayet, B., Vikkula, M.
BMJ Publishing Group
Published 2018