Candidate genes and biological processes in de novo CNVs from autistic individuals
Κύριοι συγγραφείς: | Noh, H, Marshall, C, Pinto, D, Scherer, S, Ponting, C, Webber, C |
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Μορφή: | Journal article |
Έκδοση: |
2010
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Παρόμοια τεκμήρια
Παρόμοια τεκμήρια
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46% of individuals with ASD that harbour de novo CNVs have at least one de novo CNV that overlaps a gene associated with synaptic signalling
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Forging links between human mental retardation-associated CNVs and mouse gene knockout models.
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Accurate distinction of pathogenic from benign CNVs in mental retardation.
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Forging links between human mental retardation-associated CNVs and mouse gene knockout models.
ανά: Caleb Webber, κ.ά.
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Analysis of parental origin of de novo pathogenic CNVs in patients with intellectual disability
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