. . . . . . . . . . . . "[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 . "2016-05-13T12:43:28+02:00"^^ . . . . . . . . . . . "v4.0.0.0" . "v4.0.0" .