Weisz-Hubshman, M., Burrage, L. C., Jangam, S. V., Rosenfeld, J. A., Hardenberg, S. v., Bergmann, A., . . . Lee, B. (2025). De novo variants in RYBP are associated with a severe neurodevelopmental disorder and congenital anomalies. Genetics in medicine, 27(4), . https://doi.org/10.1016/j.gim.2025.101369
Chicago Style (17th ed.) CitationWeisz-Hubshman, Monika, et al. "De Novo Variants in RYBP Are Associated with a Severe Neurodevelopmental Disorder and Congenital Anomalies." Genetics in Medicine 27, no. 4 (2025). https://doi.org/10.1016/j.gim.2025.101369.
MLA (9th ed.) CitationWeisz-Hubshman, Monika, et al. "De Novo Variants in RYBP Are Associated with a Severe Neurodevelopmental Disorder and Congenital Anomalies." Genetics in Medicine, vol. 27, no. 4, 2025, https://doi.org/10.1016/j.gim.2025.101369.