Abnormal primary and permanent dentitions with ectodermal symptoms predict WNT10A deficiency.
| Autor: | Bergendal, Birgitta1,2 birgitta.bergendal@rjl.se, Norderyd, Johanna1,2, Xiaolei Zhou3,4, Klar, Joakim3,4, Dahl, Niklas3,4 |
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| Zdroj: | BMC Medical Genetics. 11/24/2016, Vol. 17, p1-7. 7p. |
| Databáze: | Academic Search Ultimate |
| Externí odkaz: |
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