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Gerits, A., Nieminen, P., De Muynck, S. and Carels, C. (2006) Exclusion of coding region mutations in MSX1, PAX9 and AXIN2 in eight patients with severe oligodontia phenotype. Orthodontics & Craniofacial Research, 9, 129-136. doi:10.1111/j.1601-6343.2006.00367.x

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