Additional Metadata
Keywords autosomal recessive disorder, cleft face, face dysmorphia, gene mutation homozygosity, human, hypertelorism, letter, loss of function mutation, priority journal, protein alx 3, sibling, transcription factor, unclassified drug
Persistent URL dx.doi.org/10.1597/10-022.1, hdl.handle.net/1765/20643
Citation
Twigg, S.R.F., Wilkie, A.O.M., Versnel, S.L., & Mathijssen, I.M.J.. (2010). Letters to the editor. Cleft Palate - Craniofacial Journal, 47(4), 430–431. doi:10.1597/10-022.1