Identification of chromosome 7 inversion breakpoints in an autistic family narrows candidate region for autism susceptibility

Author:

Cukier Holly N.,Skaar David A.,Rayner-Evans Melissa Y.,Konidari Ioanna,Whitehead Patrice L.,Jaworski James M.,Cuccaro Michael L.,Pericak-Vance Margaret A.,Gilbert John R.

Publisher

Wiley

Subject

Genetics(clinical),Clinical Neurology,General Neuroscience

Reference47 articles.

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2. The prevalence of gilles de la tourette's syndrome in children and adolescents with autism;Baron-Cohen;Journal of Child Psychology and Psychiatry, and Allied Disciplines,1999

3. An autosomal genomic screen for autism. collaborative linkage study of autism;Barrett;American Journal of Medical Genetics,1999

4. De novo balanced translocation t (7;16) (p221; p11.2) associated with autistic disorder;Bayou;Journal of Biomedicine & Biotechnology,2008

5. Tourette syndrome in a pedigree with a 7;18 translocation: Identification of a YAC spanning the translocation breakpoint at 18q22.3;Boghosian-Sell;American Journal of Human Genetics,1996

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