Novel RAI1 :c.2736delC Variant in Smith–Magenis Syndrome: Identification by Whole Genome Sequencing and Joint Analysis.

MLA

Cuk, Mario, et al. “Novel RAI1 :C.2736delC Variant in Smith–Magenis Syndrome: Identification by Whole Genome Sequencing and Joint Analysis.” Journal of Personalized Medicine, vol. 14, no. 9, Sept. 2024, p. 901. EBSCOhost, https://doi.org/10.3390/jpm14090901.

APA

Cuk, M., Unal, B., Jandric, N., Hayes, C. P., Walker, M., Abraamyan, F., Gornik, K. C., & Ghazani, A. A. (2024). Novel RAI1 :c.2736delC Variant in Smith–Magenis Syndrome: Identification by Whole Genome Sequencing and Joint Analysis. Journal of Personalized Medicine, 14(9), 901. https://doi.org/10.3390/jpm14090901

Chicago

Cuk, Mario, Busra Unal, Nives Jandric, Connor P. Hayes, McKenzie Walker, Feruza Abraamyan, Kristina Crkvenac Gornik, and Arezou A. Ghazani. 2024. “Novel RAI1 :C.2736delC Variant in Smith–Magenis Syndrome: Identification by Whole Genome Sequencing and Joint Analysis.” Journal of Personalized Medicine 14 (9): 901. doi:10.3390/jpm14090901.