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Original article
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

Authors

  1. Correspondence to Professor Miikka Vikkula, Human Molecular Genetics, de Duve Institute, University of Louvain, Brussels 1348, Belgium; miikka.vikkula{at}uclouvain.be
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Citation

Basha M, Demeer B, Revencu N, et al
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

Publication history

  • Received October 13, 2017
  • Revised February 2, 2018
  • Accepted February 12, 2018
  • First published March 2, 2018.

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