A functional genetic link between distinct developmental language disorders

Vernes, Sonja C., Newbury, Dianne F., Abrahams, Brett S., Winchester, Laura, Nicod, Jérôme, Groszer, Matthias, Alarcón, Maricela, Oliver, Peter L. +4 more·2008·New England Journal of Medicine

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  28. Developmental language disorder – heritability and genetic correlations with other disorders affecting language
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  64. The universal basis of local linguistic exceptionality
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  65. Developmental Language Disorders
    Doris A. Trauner, Ruth D Nass · 2017 · Elsevier eBooks
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  69. Apraxia of Speech in Children and Adolescents: Applications of Neuroscience to Differential Diagnosis and Intervention
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  71. Genetic variation and individual differences in language
    Jennifer B. Misyak, Morten H. Christiansen · 2011 · Trends in language acquisition research
  72. Specific Language Impairment: Processing Deficits in Linguistic, Cognitive, and Sensory Domains
    Laurence B. Leonard, Christine M. Weber-Fox · 2012
  73. FOXP2 gene deletion and infant feeding difficulties: a case report
    Emily Zimmerman, Jill L. Maron · 2015 · Molecular Case Studies
  74. Ancient regulatory evolution shapes individual language abilities in present-day humans
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  76. Genetic Pathways Implicated in Speech and Language
    Sonja C. Vernes, Simon E. Fisher · 2013 · Springer eBooks
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    John J.M., Hakon Hakonarso · 2011 · InTech eBooks
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  80. Developmental Language Disorders
    Ruth D Nass, Doris A. Trauner · 2012 · Elsevier eBooks
  81. Modelling developmental disorders
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  83. Genetic Etiology of Autism
    Agnes Cristina, Ana Lúiza, Patricia Pereira-Nascimento · 2013 · InTech eBooks
  84. Genetic Overlaps in Mental Retardation, Autism and Schizophrenia
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  85. Advances and Challenges in the Genetics of Autism
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  88. A common genetic variant in the Neurexin family member CNTNAP2 is related to language but not communication skills in youth with Autism Spectrum Disorder
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  89. Autism and autism spectrum disorders
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  90. Language Gene Basis for Precision Personalized Education and Liberal Education (I)
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  91. Autism Spectrum Disorder: Developmental Approaches from Infancy through Early Childhood
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  92. Contactin-associated protein-like 2 expression in SH-SY5Y cells is upregulated by a FOXP2 mutant with a shortened poly-glutamine tract
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  93. Genes: Interactions with Language on Three Levels—Inter-Individual Variation, Historical Correlations and Genetic Biasing
    Dan Dediu · 2013 · The frontiers collection
  94. Paleogenomics, hominin interbreeding and language evolution.
    Antonio Benítez‐Burraco, Lluís Barceló-Coblijn · 2013 · PubMed
  95. Neurobiology of Autism Spectrum Disorders
    Gabriela Joca Martins · 2017 · Springer eBooks
  96. Biological/Biochemical Features and Molecular Genetics of Specific Language Impairment ( SLI )
    Emrah Çaylak · 2011 · Encyclopedia of Life Sciences
  97. Correction: Defining the Contribution of CNTNAP2 to Autism Susceptibility
    Srirangan Sampath, Shambu Bhat, Simone Gupta, Ashley O’Connor, Andrew B. West, Dan E. Arking, Aravinda Chakravarti · 2013 · PLoS ONE
  98. Dynamic assessment and informed intervention for children with language impairment
    Natalie Hasson · 2011 · City Research Online (City University London)
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