The common inversion of the Williams–Beuren syndrome region at 7q11.23 does not cause clinical symptoms
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference48 articles.
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2. 1.5 Mb de novo 22q11.21 microduplication in a patient with cognitive deficits and dysmorphic facial features;Alberti;Clin Genet,2007
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