Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleMutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia.AuthorsPlaisancié, Julie; Bailleul‐Forestier, Isabelle; Gaston, Véronique; Vaysse, Fréderic; Lacombe, Didier; Holder‐Espinasse, Muriel; Abramowicz, Marc; Coubes, Christine; Plessis, Ghislaine; Faivre, Laurence; Demeer, Bénédicte; Vincent‐Delorme, Catherine; Dollfus, Hélène; Sigaudy, Sabine; Guillén‐Navarro, Encarna; Verloes, Alain; Jonveaux, Philippe; Martin‐Coignard, Dominique; Colin, Estelle; Bieth, EricPublicationAmerican Journal of Medical Genetics. Part A, 2013, Vol 161A, Issue 4, p671ISSN1552-4825Publication typeArticleDOI10.1002/ajmg.a.35747