1. Dixon MJ, Haan E, Baker E, David D, McKenzie N, Williamson R, Mulley J, Farrall M, and Callen D. Association of Treacher Collins syndrome and translocation 6p21.31/16p13.11: exclusion of the locus from these candidate regions. Am J Hum Genet 1991a;48:274–80.
2. Dixon MJ, Read AP, Donnai D, Colley A, Dixon J, and Williamson R. The gene for Treacher Collins syndrome maps to the long arm of chromosome 5. Am J Hum Genet 1991b;49:17–22.
3. Collins ET. Cases with symmetrical congenital notches in the outer part of each lid and defective development of the malar bones. Trans Ophthalmol Soc UK 1900;20:190–92.
4. Dixon MJ, Dixon J, Houseal T, Bhatt M, Ward DC, Klinger K, and Landes GM. Narrowing the position of the Treacher Collins syndrome gene locus to a small interval between three new microsatellite markers at 5q32-33.1. Am J Hum Genet 1993;52:907–14.
5. Dixon J, Hovanes K, Shiang R, and Dixon MJ. Sequence analysis, identification of evolutionary conserved motifs and expression analysis of murine tcof1 provide further evidence for a potential function for the gene and its human homologue, TCOF1. Hum Mol Genet 1997;6(5):727–37.