A de novo 2q37.2 deletion encompassing AGAP1 and SH3BP4 in a patient with autism and intellectual disability. [electronic resource]

By: Contributor(s): Producer: 20200312Description: 103586 p. digitalISSN:
  • 1878-0849
Subject(s): Online resources: In: European journal of medical genetics vol. 62
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Publication Type: Case Reports; Journal Article

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