Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Ectodermal Dysplasia and AXIN2[original query] |
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Isolated oligodontia associated with mutations in EDARADD, AXIN2, MSX1, and PAX9 genes. American journal of medical genetics. Part A 2011 Jul 155A (7): 1616-22. Bergendal Birgitta, Klar Joakim, Stecksén-Blicks Christina, Norderyd Johanna, Dahl Nikl |
Mutations in WNT10A are present in more than half of isolated hypodontia cases. Journal of medical genetics 2012 May 49 (5): 327-31. van den Boogaard Marie-José, Créton Marijn, Bronkhorst Yvon, van der Hout Annemieke, Hennekam Eric, Lindhout Dick, Cune Marco, Ploos van Amstel Hans Kristi |
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