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N Hoppman-Chaney, K Wain, PR Seger, DW Superneau and JC Hodge Identification of single gene deletions at 15q13.3: further evidence that CHRNA7 causes the 15q13.3 microdeletion syndrome phenotype Clinical Genetics 83

Article first published online: 7 AUG 2012 | DOI: 10.1111/j.1399-0004.2012.01925.x

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