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  1. The 15q24 microdeletion syndrome has been recently described as a recurrent, submicroscopic genomic imbalance found in individuals with intellectual disability, typical facial appearance, hypotonia, and digita...

    Authors: L Alison McInnes, Alisa Nakamine, Marion Pilorge, Tracy Brandt, Patricia Jiménez González, Marietha Fallas, Elina R Manghi, Lisa Edelmann, Joseph Glessner, Hakon Hakonarson, Catalina Betancur and Joseph D Buxbaum
    Citation: Molecular Autism 2010 1:5
    Content type: Research Published on:

  2. Autism is a complex disorder characterized by deficits involving communication, social interaction, and repetitive and restrictive patterns of behavior. Twin studies have shown that autism is strongly heritabl...

    Authors: Jerome Carayol, Gerard D Schellenberg, Frederic Tores, Jörg Hager, Andreas Ziegler and Geraldine Dawson
    Citation: Molecular Autism 2010 1:4
    Content type: Research Published on:

  3. It has been suggested that efforts to identify genetic risk markers of autism spectrum disorder (ASD) would benefit from the analysis of more narrowly defined ASD phenotypes. Previous research indicates that '...

    Authors: Dale S Cannon, Judith S Miller, Reid J Robison, Michele E Villalobos, Natalie K Wahmhoff, Kristina Allen-Brady, William M McMahon and Hilary Coon
    Citation: Molecular Autism 2010 1:3
    Content type: Research Published on:

  4. Autism is a neurodevelopmental disorder which is known to have a strong genetic component and is most likely oligogenic. However, the necessary role of environmental factors has been well documented. Prior res...

    Authors: Roksana Sasanfar, Stephen A Haddad, Ala Tolouei, Majid Ghadami, Dongmei Yu and Susan L Santangelo
    Citation: Molecular Autism 2010 1:2
    Content type: Research Published on:
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Molecular Autism

ISSN: 2040-2392