Identification of single gene deletions at 15q13.3: further evidence that CHRNA7 causes the 15q13.3 microdeletion syndrome phenotype. [electronic resource]

By: Contributor(s): Producer: 20140114Description: 345-51 p. digitalISSN:
  • 1399-0004
Subject(s): Online resources: In: Clinical genetics vol. 83
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't

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