Towards a molecular characterization of autism spectrum disorders: an exome sequencing and systems approach.

An, J Y; Cristino, A S; Zhao, Q; Edson, J; Williams, S M; Ravine, D; Wray, J; Marshall, V M; Hunt, A; Whitehouse, A J O; Claudianos, C

An, J Y; Cristino, A S; Zhao, Q; Edson, J; Williams, S M; Ravine, D; Wray, J; Marshall, V M; Hunt, A; Whitehouse, A J O; Claudianos, C.

Afiliación

An JY; Queensland Brain Institute, The University of Queensland, Brisbane, QLD, Australia.
Cristino AS; Queensland Brain Institute, The University of Queensland, Brisbane, QLD, Australia.
Zhao Q; Queensland Brain Institute, The University of Queensland, Brisbane, QLD, Australia.
Edson J; Queensland Brain Institute, The University of Queensland, Brisbane, QLD, Australia.
Williams SM; Queensland Brain Institute, The University of Queensland, Brisbane, QLD, Australia.
Ravine D; School of Pathology and Laboratory Medicine, Perth, WA, Australia.
Wray J; State Child Development Centre, Child and Adolescent Health Service, Princess Margaret Hospital for Children, Perth, WA, Australia.
Marshall VM; Queensland Brain Institute, The University of Queensland, Brisbane, QLD, Australia.
Hunt A; Telethon Institute for Child Health Research, Centre for Child Health Research, University of Western Australia, Subiaco, WA, Australia.
Whitehouse AJ; 1] Telethon Institute for Child Health Research, Centre for Child Health Research, University of Western Australia, Subiaco, WA, Australia [2] Cooperative Research Centre for Living with Autism Spectrum Disorders (Autism CRC), Brisbane, QLD, Australia.
Claudianos C; 1] Queensland Brain Institute, The University of Queensland, Brisbane, QLD, Australia [2] Cooperative Research Centre for Living with Autism Spectrum Disorders (Autism CRC), Brisbane, QLD, Australia.

Transl Psychiatry ; 4: e394, 2014 Jun 03.

Article en En | MEDLINE | ID: mdl-24893065

Asunto(s)

Trastornos Generalizados del Desarrollo Infantil/genética; Exoma/genética; Variación Genética/genética; Sistema de Registros; Adulto; Niño; Femenino; Redes Reguladoras de Genes/genética; Predisposición Genética a la Enfermedad; Humanos; Masculino; Molécula L1 de Adhesión de Célula Nerviosa/genética; Fenotipo

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Variación Genética / Trastornos Generalizados del Desarrollo Infantil / Sistema de Registros / Exoma Tipo de estudio: Prognostic_studies Límite: Adult / Child / Female / Humans / Male Idioma: En Revista: Transl Psychiatry Año: 2014 Tipo del documento: Article País de afiliación: Australia Pais de publicación: Estados Unidos

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