A de novo 14q12q13.3 interstitial deletion in a patient affected by a severe neurodevelopmental disorder of unknown origin. [electronic resource]

By: Contributor(s): Producer: 20120604Description: 689-93 p. digitalISSN:
  • 1552-4833
Subject(s): Online resources: In: American journal of medical genetics. Part A vol. 158A
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Publication Type: Letter; Research Support, Non-U.S. Gov't

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