A novel PITX2 mutation in non-syndromic orodental anomalies.
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DOI: 10.1111/odi.12804
Abstract: OBJECTIVE To identify orodental characteristics and genetic aetiology of a family affected with non-syndromic orodental anomalies. SUBJECTS AND METHODS Physical and oral features were characterised. DNA was collected from an affected Thai family. Whole-exome sequencing… read more here.
Keywords: orodental anomalies; non syndromic; novel pitx2; pitx2 mutation ... See more keywords