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De Novo Heterozygous Mutations in SMC3 Cause a Range of Cornelia de Lange Syndrome‐Overlapping Phenotypes

Overview of attention for article published in Human Mutation, March 2015
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Mentioned by

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2 X users
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1 Facebook page

Citations

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79 Dimensions

Readers on

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90 Mendeley
Summary X Facebook Dimensions citations
So far, Dimensions has found 79 publications that cite this research output.

79

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