Clinical report: inherited deletion of chromosome 12q21.31q21.32 associated with a distinct phenotype and intellectual disability. [electronic resource]

By: Contributor(s): Producer: 20160620Description: 151-5 p. digitalISSN:
  • 1473-5717
Subject(s): Online resources: In: Clinical dysmorphology vol. 24
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Publication Type: Case Reports; Journal Article

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