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Publication : De novo Xq11.11 microdeletion including ARHGEF9 in a boy with mental retardation, epilepsy, macrosomia, and dysmorphic features.

First Author  Lesca G Year  2011
Journal  Am J Med Genet A Volume  155A
Issue  7 Pages  1706-11
PubMed ID  21626670 Mgi Id 
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