Identification of single gene deletions at 15q13.3: further evidence that CHRNA7 causes the 15q13.3 microdeletion syndrome phenotype
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K. Wain | Jennelle C Hodge | N. Hoppman-Chaney | PR Seger | DW Superneau | JC Hodge | Jennelle C. Hodge | Karen E. Wain