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Tbx1: identification of a 22q11.2 gene as a risk factor for autism spectrum disorder in a mouse model

  • Published:2011-09-09 Issue:24 Volume:20 Page:4775-4785
  • ISSN:1460-2083
  • Container-title:Human Molecular Genetics
  • language:en
  • Short-container-title:

Author:

Hiramoto Takeshi,Kang Gina,Suzuki Go,Satoh Yasushi,Kucherlapati Raju,Watanabe Yasuhiro,Hiroi Noboru

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Reference80 articles.

1. A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden;Steffenburg;J. Child Psychol. Psychiatry,1989

2. Autism as a strongly genetic disorder: evidence from a British twin study;Bailey;Psychol. Med.,1995

3. Solving the autism puzzle a few pieces at a time;Schaaf;Neuron,2011

4. Velo-cardio-facial syndrome: language and psychological profiles;Golding-Kushner;J. Craniofac. Genet. Dev. Biol.,1985

5. Adolescents and young adults with 22q11 deletion syndrome: psychopathology in an at-risk group;Baker;Br. J. Psychiatry,2005
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