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Abnormal primary and permanent dentitions with ectodermal symptoms predict WNT10A deficiency

Journal Article published 24 Nov 2016 in BMC Medical Genetics volume 17 issue 1

Research funded by Medicinska Forskningsrådet (2015-02424) | Thuréus foundation for oral and dental research

Authors: Birgitta Bergendal, Johanna Norderyd, Xiaolei Zhou, Joakim Klar, Niklas Dahl