Search Results - Cechner, K.

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    Novel DNMT3A germline mutations are associated with inherited Tatton‐Brown–Rahman syndrome

    Novel DNMT3A germline mutations are associated with inherited Tatton‐Brown–Rahman syndrome by Xin, B., Cruz Marino, T., Szekely, J., Leblanc, J., Cechner, K., Sency, V., Wensel, C., Barabas, M., Therriault, V., Wang, H.

    Published in Clinical genetics
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