Cite
HARVARD Citation
Brand, F. et al. (2022). Next‐generation phenotyping contributing to the identification of a 4.7 kb deletion in KANSL1 causing Koolen‐de Vries syndrome. Human mutation. 43 (11), pp. 1659-1665. [Online].
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Brand, F. et al. (2022). Next‐generation phenotyping contributing to the identification of a 4.7 kb deletion in KANSL1 causing Koolen‐de Vries syndrome. Human mutation. 43 (11), pp. 1659-1665. [Online].