Cite
HARVARD Citation
Goldenberg, A. et al. (2016). Clinical and molecular findings in 39 patients with KBG syndrome caused by deletion or mutation of ANKRD11. American journal of medical genetics. 170 (11), pp. 2847-2859. [Online].
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Goldenberg, A. et al. (2016). Clinical and molecular findings in 39 patients with KBG syndrome caused by deletion or mutation of ANKRD11. American journal of medical genetics. 170 (11), pp. 2847-2859. [Online].