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

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Bibliographic Details
Published in:European journal of human genetics : EJHG 2019, Vol.27 (1)
Main Authors: Basha, M., Demeer, Bénédicte, Revencu, N., Theys, S., Saba, S. Bou, Boute, O., Devauchelle, Bernard, Francois, G., Bayet, B., Vikkula, M.
Format: Article
Language:English
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Life Sciences
Online Access:Get full text
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ISSN:1018-4813
1476-5438