. . . . . . . . . . . . "[In this study of a 14-yr-old boy with typical cleidocranial dysplasia phenotype, the authors found a novel CBFA1/RUNX2 gene mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2009-03-31"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2015-08-25T14:39:43+02:00"^^ . . . . . . . . . . . "v3.0.0.0" . "v3.0.0" .