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APA Citation
Fry, D., Groepper, D., MacCarrick, G., Demo, E. M., Thomas, M. J., Wilkes, M. J., Lyons, M. J., Tucker, M. E., Steding, C., & Fleischer, J. (2022). loeys–Dietz syndrome caused by 1q41 deletion including TGFB2 is associated with a neurodevelopmental phenotype. American journal of medical genetics, 188(7), 2237–2241. http://access.bl.uk/ark:/81055/vdc_100158007767.0x000033