Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia (Q34134692)
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English | Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia |
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Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia (English)
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Fritz Poustka
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Alistair T Pagnamenta
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Elena Bacchelli
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Maretha V de Jonge
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Ghazala Mirza
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Thomas S Scerri
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Fiorella Minopoli
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Andreas Chiocchetti
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Kerstin U Ludwig
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Ernesto Lowy
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Jade A Chapman
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Sabine M Klauck
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Renske H Houben
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Wouter G Staal
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Roel A Ophoff
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Julie Williams
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Jiannis Ragoussis
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Anthony J Bailey
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Elena Maestrini
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International Molecular Genetic Study Of Autism Consortium
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26 March 2010
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68
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320-328
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