Novel Mutation of Cleidocranial Dysplasia-related Frameshift Runt-related Transcription Factor 2 in a Sporadic Chinese Case. [electronic resource]

By: Contributor(s): Producer: 20170313Description: 165-170 p. digitalISSN:
  • 2542-5641
Subject(s): Online resources: In: Chinese medical journal vol. 130
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Publication Type: Case Reports; Journal Article

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