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
BMJ Publishing Group
Published 2018
Publication Date: |
2018-06-26
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Publisher: |
BMJ Publishing Group
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Print ISSN: |
0022-2593
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Electronic ISSN: |
1468-6244
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Topics: |
Medicine
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Keywords: |
Editor's choice
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Published by: |