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Department of Psychiatry
Shambhu Bhat has not added Biography.
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A novel in-frame deletion in ARX is associated with lissencephaly with absent corpus callosum and hypoplastic genitalia.
American journal of medical genetics. Part A Sep, 2005 | Pubmed ID: 16097002
Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation.
Nature genetics Sep, 2007 | Pubmed ID: 17704778
Evidence that SIZN1 is a candidate X-linked mental retardation gene.
American journal of medical genetics. Part A Oct, 2008 | Pubmed ID: 18798319
Intellectual disability, midface hypoplasia, facial hypotonia, and Alport syndrome are associated with a deletion in Xq22.3.
American journal of medical genetics. Part A Mar, 2010 | Pubmed ID: 20186809
University of Maryland School of Medicine
Adem Can*,1,
David T. Dao*,1,2,
Chantelle E. Terrillion3,
Sean C. Piantadosi1,
Shambhu Bhat1,
Todd D. Gould1,3,4
1Department of Psychiatry, University of Maryland School of Medicine,
2, Tulane University School of Medicine,
3The Program in Neuroscience, University of Maryland ,
4Department of Pharmacology and Experimental Therapeutics, University of Maryland School of Medicine
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