A novel RAD21 variant associated with intrafamilial phenotypic variation in Cornelia de Lange syndrome - review of the literature. [electronic resource]

By: Contributor(s): Producer: 20170630Description: 647-649 p. digitalISSN:
  • 1399-0004
Subject(s): Online resources: In: Clinical genetics vol. 91
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Publication Type: Case Reports; Letter

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