A patient with de novo 0.45 Mb deletion of 2p16.1: the role of BCL11A, PAPOLG, REL, and FLJ16341 in the 2p15-p16.1 microdeletion syndrome. [electronic resource]

By: Contributor(s): Producer: 20130909Description: 865-70 p. digitalISSN:
  • 1552-4833
Subject(s): Online resources: In: American journal of medical genetics. Part A vol. 161A
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

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