Unknown diagnosis in two male cousins with facial abnormalities, optic atrophy, abnormal EEG, and severe psychomotor retardation. [electronic resource]

By: Producer: 20030908Description: 381-4 p. digitalISSN:
  • 1552-4825
Subject(s): Online resources: In: American journal of medical genetics. Part A vol. 116A
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

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