Report of two patients and further characterization of interstitial 9p13 deletion--a rare but recurrent microdeletion syndrome? [electronic resource]

By: Contributor(s): Producer: 20121109Description: 2328-35 p. digitalISSN:
  • 1552-4833
Subject(s): Online resources: In: American journal of medical genetics. Part A vol. 158A
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Publication Type: Case Reports; Journal Article

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