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, 2018)
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