Cite
HARVARD Citation
Boone, P. et al. (2020). Biallelic mutation of FBXL7 suggests a novel form of Hennekam syndrome. American journal of medical genetics. 182 (1), pp. 189-194. [Online].
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Boone, P. et al. (2020). Biallelic mutation of FBXL7 suggests a novel form of Hennekam syndrome. American journal of medical genetics. 182 (1), pp. 189-194. [Online].