A new cohort of MECP2 mutation screening in unexplained mental retardation: careful re-evaluation is the best indicator for molecular diagnosis. [electronic resource]

By: Contributor(s): Producer: 20060928Description: 1603-7 p. digitalISSN:
  • 1552-4825
Subject(s): Online resources: In: American journal of medical genetics. Part A vol. 140
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Publication Type: Letter; Research Support, Non-U.S. Gov't

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