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The roles of FMRP-regulated genes in autism spectrum disorder: single- and multiple-hit genetic etiologies.
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Recognition of face and non-face stimuli in autistic spectrum disorder.
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In: Autism Res , 6 (6) 550 - 560. (2013) (2013)
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Event narratives in 11-14 year olds with autistic spectrum disorder
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In: International Journal of Language & Communication Disorders , 48 (5) pp. 522-533. (2013) (2013)
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Deficits in volitional oculomotor control align with language status in autism spectrum disorders.
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In: Dev Sci , 16 (1) pp. 56-66. (2013) (2013)
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Sylvian fissure and parietal anatomy in children with autism spectrum disorder
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Individual common variants exert weak effects on the risk for autism spectrum disorders.
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In: Human molecular genetics, vol 21, iss 21 (2012)
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Survey of the Assessment Methods Used in Texas Public Schools for the Diagnosis of Pervasive Developmental Disorders in Children
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Social use of language in children with reactive attachment disorder and autism spectrum disorders.
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In: Eur Child Adolesc Psychiatry , 21 (5) pp. 267-276. (2012) (2012)
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Individual common variants exert weak effects on the risk for autism spectrum disorderspi.
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In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef ; ORA review team (2012)
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A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.
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In: Journal of Medical Genetics, vol. 49, no. 10, pp. 660-668 (2012)
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Teacher Implemented Pivotal Response Training To Improve Communication In Children With Autism Spectrum Disorders
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Autism, language and communication in children with sex chromosome trisomies.
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In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2011)
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Accessing and selecting word meaning in autism spectrum disorder.
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Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders.
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In: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, vol 153B, iss 4 (2010)
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Association Between a High-Risk Autism Locus on 5p14 and Social Communication Spectrum Phenotypes in the General Population
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In: AM J PSYCHIAT , 167 (11) 1364 - 1372. (2010) (2010)
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Congenital perisylvian dysfunction - is it a spectrum?
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In: Dev Med Child Neurol , 52 (1) pp. 33-39. (2010) (2010)
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Comunicação aumentativa e alternativa para sujeitos com transtornos globais do desenvolvimento na promoção da expressão e intencionalidade por meio de ações mediadoras
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Comunicação aumentativa e alternativa para sujeitos com transtornos globais do desenvolvimento na promoção da expressão e intencionalidade por meio de ações mediadoras
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