Linkage and candidate gene studies of autism spectrum disorders in European populations.

Linkage and candidate gene studies of autism spectrum disorders in European populations.

Over the past decade, research on the genetic variants underlying susceptibility to autism and autism spectrum disorders (ASDs) has focused on linkage and candidate gene studies. This research has implicated various chromosomal loci and genes. Candidate gene studies have proven to be particularly in...

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Bibliografische gegevens
Hoofdauteurs:	Holt, R, Barnby, G, Maestrini, E, Bacchelli, E, Brocklebank, D, Sousa, I, Mulder, E, Kantojärvi, K, Järvelä, I, Klauck, S, Poustka, F, Bailey, A, Monaco, A
Formaat:	Journal article
Taal:	English
Gepubliceerd in:	2010

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Molecular genetic investigations of autism.
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MET and autism susceptibility: family and case-control studies
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Response to paper by Molloy et al.: linkage on 21q and 7q in autism subset with regression.
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A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium.
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