1p13.2 deletion displays clinical features overlapping Noonan syndrome, likely related to NRAS gene haploinsufficiency

Overview of attention for article published in Genetics and Molecular Biology, August 2016

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A novel 1p13.2 deletion associates with neurodevelopmental disorders in a three-generation pedigree

Article in BMC Medical Genomics (May 2023)

Multifunctional requirements for ERK1/2 signaling in the development of ganglionic eminence derived glia and cortical inhibitory neurons

Preprint in bioRxiv (August 2022)

Bilateral squamosal synostosis: unusual presentation of chromosome 1p12–1p13.3 deletion. Illustrative case

Article in Journal of Neurosurgery Case Lessons (January 2021)

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