Mutation screening of the 3q29 microdeletion syndrome candidate genes DLG1 and PAK2 in schizophrenia
Author:
Publisher
Wiley
Subject
Cellular and Molecular Neuroscience,Psychiatry and Mental health,Genetics(clinical)
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.b.31231/fullpdf
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4. Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication;Ballif;Mol Cytogenet,2008
5. Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence;Benko;Nat Genet,2009
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