Publications
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Author Title [ Year
] Filters: Keyword is Cyclin-Dependent Kinase Inhibitor p21 [Clear All Filters]
Mutations in EBF3 Disturb Transcriptional Profiles and Cause Intellectual Disability, Ataxia, and Facial Dysmorphism. Am J Hum Genet 100, 117-127 (2017).
FOXE3 mutations predispose to thoracic aortic aneurysms and dissections. J Clin Invest 126, 948-61 (2016).
