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Tourette syndrome in a pedigree with a 7;18 translocation: identification of a YAC spanning the translocation breakpoint at 18q22.3.

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References

1986The Inheritance of Gilles de la Tourette's Syndrome and Associated Behaviors493 cited
2022A Family Study of Gilles de la Tourette Syndrome317 cited
1996Polygenic inheritance of Tourette syndrome, stuttering, attention deficit hyperactivity, conduct, and oppositional defiant disorder: The additive and subtractive effect of the three dopaminergic genes—DRD2, DβH, and DAT1270 cited
1993Evidence for Autosomal Dominant Transmission in Tourette's Syndrome189 cited
1990An epidemiologic study of Tourette's syndrome in a single school district.179 cited
1984Detection of major gene for Gilles de la Tourette syndrome.120 cited
1986A Prevalence Study of Gilles de la Tourette Syndrome in North Dakota School-Age Children103 cited
1994Bilineal transmission in Tourette's syndrome families98 cited

Cited by

2004Neurobiology and neuroimmunology of Tourette?s syndrome: an update90 cited
1999The Genetics of Tourette Syndrome82 cited
2003Epigenetic abnormalities associated with a chromosome 18(q21-q22) inversion and a Gilles de la Tourette syndrome phenotype81 cited
2011Translocation breakpoint at 7q31 associated with tics: further evidence for IMMP2L as a candidate gene for Tourette syndrome78 cited
2014Intragenic deletions affecting two alternative transcripts of the IMMP2L gene in patients with Tourette syndrome71 cited

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2006Genetics and Epidemiology of Tourette Syndrome67 cited