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<http://identifiers.org/pubmed/21549343> <http://purl.org/dc/terms/title> "Whole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndrome" <http://purl.org/np/RAHzPjp4VbWStUUmvfSsEBPP20RqR-UnqLqefKeSwsVLU#provenance> .
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