DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Plaisancié J, Bailleul-Forestier I, Gaston V , et al.
Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia.
Am J Med Genet A 2013;
161A (4) 671-678
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