Vetrini, F., McKee, S., Rosenfeld, J. A., Suri, M., Lewis, A. M., Nugent, K. M., . . . Liu, P. (2019). Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome. Genome Med.
Citação norma ChicagoVetrini, Francesco, et al. "Correction To: De Novo and Inherited TCF20 Pathogenic Variants Are Associated With Intellectual Disability, Dysmorphic Features, Hypotonia, and Neurological Impairments With Similarities to Smith–Magenis Syndrome." Genome Med 2019.
Citação norma MLAVetrini, Francesco, et al. "Correction To: De Novo and Inherited TCF20 Pathogenic Variants Are Associated With Intellectual Disability, Dysmorphic Features, Hypotonia, and Neurological Impairments With Similarities to Smith–Magenis Syndrome." Genome Med 2019.