DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Arzoo PS, Klar J, Bergendal B, Norderyd J, Dahl N.
WNT10A mutations account for ¼ of population-based isolated oligodontia and show phenotypic correlations.
Am J Med Genet A 2014;
164A (2) 353-359
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