Cockayne syndrome caused by paternally inherited 5 Mb deletion of 10q11.2 and a frameshift mutation of ERCC6. [electronic resource]

By: Contributor(s): Producer: 20110928Description: 272-6 p. digitalISSN:
  • 1878-0849
Subject(s): Online resources: In: European journal of medical genetics vol. 54
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Publication Type: Case Reports; Journal Article

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