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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, Mirta, Demeer, Bénédicte, Revencu, Nicole, Helaers, Raphael, Theys, Stephanie, Bou Saba, Sami, Boute, Odile, Devauchelle, Bernard, Francois, Geneviève, Bayet, Bénédicte, Vikkula, MiikkaLanguage:
english
Journal:
Journal of Medical Genetics
DOI:
10.1136/jmedgenet-2017-105110
Date:
March, 2018
File:
PDF, 4.16 MB
english, 2018