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De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome

Overview of attention for article published in Genome Medicine, February 2019
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Mentioned by

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4 X users
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1 Facebook page

Citations

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26 Dimensions

Readers on

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85 Mendeley
citeulike
2 CiteULike
Summary X Facebook Dimensions citations
So far, Dimensions has found 26 publications that cite this research output.

26

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