A Boy with Holt-Oram Syndrome Caused by Novel Mutation c.1304delT in the TBX5 Gene. [electronic resource]

By: Contributor(s): Publication details: Molecular syndromology Sep 2011Description: 307-310 p. digitalISSN:
  • 1661-8769
Online resources: In: Molecular syndromology vol. 1
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Publication Type: Journal Article

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