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Exclusion of coding region mutations in MSX1, PAX9 and AXIN2 in eight patients with severe oligodontia phenotype
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A. Gerits, P. Nieminen, S. De Muynck, and C. Carels Exclusion of coding region mutations in MSX1, PAX9 and AXIN2 in eight patients with severe oligodontia phenotype Orthod Craniofac Res 9 3 2006 129 136
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(2006)
Orthod Craniofac Res
, vol.9
, Issue.3
, pp. 129-136
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Gerits, A.1
Nieminen, P.2
De Muynck, S.3
Carels, C.4
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