Disruption of a Novel Gene (IMMP2L) by a Breakpoint in 7q31 Associated with Tourette Syndrome

This publication has 27 references indexed in Scilit:

• Degenerate oligonucleotide-primed PCR: General amplification of target DNA by a single degenerate primer
  Published by Elsevier ,2004
• Significant Linkage for Tourette Syndrome in a Large French Canadian Family
  American Journal of Human Genetics, 2000
• Identification of a Novel Gene on Chromosome 7q31 That Is Interrupted by a Translocation Breakpoint in an Autistic Individual
  American Journal of Human Genetics, 2000
• The SPCH1 Region on Human 7q31: Genomic Characterization of the Critical Interval and Localization of Translocations Associated with Speech and Language Disorder
  American Journal of Human Genetics, 2000
• An international perspective on Tourette syndrome: selected findings from 3500 individuals in 22 countries
  Developmental Medicine and Child Neurology, 2000
• Annotation: Gilles de la Tourette Syndrome—An Update
  Journal of Child Psychology and Psychiatry, 1994
• A Mitochondrial Protease with Two Catalytic Subunits of Nonoverlapping Specificities
  Science, 1993
• Signal peptidases in prokaryotes and eukaryotes - a new protease family
  Trends in Biochemical Sciences, 1992
• Autosomal Dominant Gene Transmission in a Large Kindred with Gilles de la Tourette Syndrome
  The British Journal of Psychiatry, 1992
• GENE LOCATION IN TOURETTE SYNDROME
  The Lancet, 1987