A novel RAD21 mutation in a boy with mild Cornelia de Lange presentation: Further delineation of the phenotype. [electronic resource]

By: Contributor(s): Producer: 20200930Description: 103620 p. digitalISSN:
  • 1878-0849
Subject(s): Online resources: In: European journal of medical genetics vol. 63
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Publication Type: Case Reports; Journal Article

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