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HARVARD Citation
Popp, B. et al. (2023). The constitutional gain‐of‐function variant p.Glu1099Lys in NSD2 is associated with a novel syndrome. Clinical genetics. 103 (2), pp. 226-230. [Online].
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Popp, B. et al. (2023). The constitutional gain‐of‐function variant p.Glu1099Lys in NSD2 is associated with a novel syndrome. Clinical genetics. 103 (2), pp. 226-230. [Online].