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

  1. Plaisancié, J.
  2. Bailleul-Forestier, I.
  3. Gaston, V.
  4. Vaysse, F.
  5. Lacombe, D.
  6. Holder-Espinasse, M.
  7. Abramowicz, M.
  8. Coubes, C.
  9. Plessis, G.
  10. Faivre, L.
  11. Demeer, B.
  12. Vincent-Delorme, C.
  13. Dollfus, H.
  14. Sigaudy, S.
  15. Guillén-Navarro, E.
  16. Verloes, A.
  17. Jonveaux, P.
  18. Martin-Coignard, D.
  19. Colin, E.
  20. Bieth, E.
  21. Calvas, P.
  22. Chassaing, N.
Journal:
American Journal of Medical Genetics, Part A

ISSN: 1552-4825 1552-4833

Year of publication: 2013

Volume: 161

Issue: 4

Pages: 671-678

Type: Article

DOI: 10.1002/AJMG.A.35747 GOOGLE SCHOLAR

Sustainable development goals