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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

9p monosomy in a patient with Gilles de la Tourette's syndrome.

Gilles de la Tourette's syndrome ( GTS) is a genetic disorder characterized by multiple motor and vocal tics, obsessive-compulsive disorder, and attention-deficit disorder. Family studies support the presence of an autosomal dominant gene; however, to date, an assignment for the GTS locus has not been made. We present the case of a boy with GTS and a deletion of the terminal portion of the short arm of chromosome 9, del(9)(qter----p2304:).[1]


  1. 9p monosomy in a patient with Gilles de la Tourette's syndrome. Taylor, L.D., Krizman, D.B., Jankovic, J., Hayani, A., Steuber, P.C., Greenberg, F., Fenwick, R.G., Caskey, C.T. Neurology (1991) [Pubmed]
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