Genome scan for linkage to Gilles de la Tourette syndrome

This publication has 31 references indexed in Scilit:

• Absence of Linkage of Phonological Coding Dyslexia to Chromosome 6p23-p21.3 in a Large Family Data Set
  American Journal of Human Genetics, 1998
• Current Status of Genetic Studies of Gilles de la Tourette Syndrome
  The Canadian Journal of Psychiatry, 1998
• No evidence for a major gene effect of the dopamine D4 receptor gene in the susceptibility to Gilles de la Tourette syndrome in five Canadian families
  American Journal of Medical Genetics, 1996
• OCD and Touretteʼs Syndrome
  Psychiatric Genetics, 1995
• The genetic susceptibility to Gilles de la Tourette Syndrome in a large multiple affected british kindred: Linkage analysis excludes a role for the genes coding for dopamine D1, D2, D3, D4, D5 receptors, dopamine beta hydroxylase, tyrosinase, and tyrosine hydroxylase
  Biological Psychiatry, 1995
• Failure to find linkage and increased homozygosity for the dopamine D3 receptor gene in Tourette's syndrome
  The Lancet, 1993
• Evidence for Autosomal Dominant Transmission in Tourette's Syndrome
  The British Journal of Psychiatry, 1993
• Association between Tourette's syndrome and homozygosity at the dopamine D3 receptor gene
  The Lancet, 1993
• Autosomal Dominant Gene Transmission in a Large Kindred with Gilles de la Tourette Syndrome
  The British Journal of Psychiatry, 1992
• Possible linkage of Tourette syndrome to markers on short arm of chromosome 3 (C3p21-14)
  The Lancet, 1990