Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia

✍ Scribed by Plaisancié, 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, Eric; Calvas, Patrick; Chassaing, Nicolas

• Book ID: 120061294
• Publisher: John Wiley and Sons
• Year: 2013
• Tongue: English
• Weight: 241 KB
• Volume: 161
• Category: Article
• ISSN: 1552-4825
• DOI: 10.1002/ajmg.a.35747