| 1 | STHAG4, WNT10A
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| WNT10A mutations account for ¼ of population-based isolated oligodontia and show phenotypic correlations.
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| Arzoo PS, Klar J, Bergendal B, Norderyd J, Dahl N.
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| Am J Med Genet A 164A(2):353-9. doi: 10.1002/ajmg.a.36243. Epub 2013 Nov 25.
2014
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| 2 | STHAG4, WNT10A
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| A novel WNT10A mutation causes non-syndromic hypodontia in an Egyptian family.
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| Abdalla EM, Mostowska A, Jagodziński PP, Dwidar K, Ismail SR.
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| Arch Oral Biol 59(7):722-8. doi: 10.1016/j.archoralbio.2014.04.004. Epub 2014 Apr 19.
2014
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| 3 | STHAG4, WNT10A
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| WNT10A variants are associated with non-syndromic tooth agenesis in the general population.
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| Song S, Zhao R, He H, Zhang J, Feng H, Lin L.
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| Hum Genet 133(1):117-24. doi: 10.1007/s00439-013-1360-x. Epub 2013 Sep 17.
2014
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| 4 | STHAG4, WNT10A
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| Mutations in WNT10A are present in more than half of isolated hypodontia cases.
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| van den Boogaard MJ, Créton M, Bronkhorst Y, van der Hout A, Hennekam E, Lindhout D, Cune M, Ploos van Amstel HK.
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| J Med Genet 49(5):327-31. doi: 10.1136/jmedgenet-2012-100750.
2012
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| 5 | STHAG4, WNT10A
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| WNT10A and isolated hypodontia.
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| Kantaputra P, Sripathomsawat W.
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| Am J Med Genet A 155A(5):1119-22. doi: 10.1002/ajmg.a.33840. Epub 2011 Apr 11.
2011
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