Whole-exome sequencing identification of a novel splicing mutation of RUNX2 in a Chinese family with cleidocranial dysplasia. [electronic resource]

By: Contributor(s): Producer: 20191212Description: 49-56 p. digitalISSN:
  • 1879-1506
Subject(s): Online resources: In: Archives of oral biology vol. 100
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Publication Type: Journal Article

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