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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,
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