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publicationName Journal of Inherited Metabolic Disease
startingPage 648
bibliographicCitation Bergwitz C, Prochnau A, Mayr B, Kramer FJ, Rittierodt M, Berten HL, Hausamen JE, Brabant G. Identification of novel CBFA1/RUNX2 mutations causing cleidocranial dysplasia. J Inherit Metab Dis. 2001 Nov;24(6):648–56. doi: 10.1023/a:1012758925617. PMID: 11768584.
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date 200111
identifier https://doi.org/10.1023/a:1012758925617
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language English
source https://pubmed.ncbi.nlm.nih.gov/
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title Identification of novel CBFA1/RUNX2 mutations causing cleidocranial dysplasia
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Total number of triples: 37.