Molecular characterization of a 12q22-q24 deletion associated with congenital deafness: confirmation and refinement of the DFNA25 locus. [electronic resource]

By: Contributor(s): Producer: 20030807Description: 122-6 p. digitalISSN:
  • 1552-4825
Subject(s): Online resources: In: American journal of medical genetics. Part A vol. 117A
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

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