Characterization of Williams-Beuren Syndrome Mouse Models: Linking Genes with Cognition and Behaviour
Deletion (Williams-Beuren syndrome (WBS)) and duplication (Dup7q11.23) of a common interval spanning 26 genes on chromosome 7q11.23 cause disorders with a spectrum of clinical, cognitive and behavioural symptoms. Studies of individuals with atypical deletions have implicated two genes, GTF2IRD1 and...
Main Author: | Lam, Emily |
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Other Authors: | Osborne, Lucy |
Language: | en_ca |
Published: |
2012
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Subjects: | |
Online Access: | http://hdl.handle.net/1807/32595 |
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