Phenotypic and molecular characterisation of CDK13-related congenital heart defects, dysmorphic facial features and intellectual developmental disorders

Overview of attention for article published in Genome Medicine, August 2017

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So far, Dimensions has found 38 publications that cite this research output.

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CHAPTER78 Genetics of Common Birth Defects in Newborns

Book chapter (January 2024)

The spreading of facultative H3K9me3-heterochromatin drives congenital disease

Preprint in bioRxiv (August 2023)

Oncogenic CDK13 mutations impede nuclear RNA surveillance

Article in Science (April 2023)

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