Cite
HARVARD Citation
Dias, C. et al. (2021). De novo variants in TCF7L2 are associated with a syndromic neurodevelopmental disorder. American journal of medical genetics. 185 (8), pp. 2384-2390. [Online].
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Dias, C. et al. (2021). De novo variants in TCF7L2 are associated with a syndromic neurodevelopmental disorder. American journal of medical genetics. 185 (8), pp. 2384-2390. [Online].