Etiology and Anatomical Variation in Treacher Collins Syndrome

Author:

Smith Francis Joel

Publisher

Springer International Publishing

Reference26 articles.

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.

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