Cuk, M.; Unal, B.; Jandric, N.; Hayes, C.P.; Walker, M.; Abraamyan, F.; Gornik, K.C.; Ghazani, A.A.
Novel RAI1:c.2736delC Variant in Smith–Magenis Syndrome: Identification by Whole Genome Sequencing and Joint Analysis. J. Pers. Med. 2024, 14, 901.
https://doi.org/10.3390/jpm14090901
AMA Style
Cuk M, Unal B, Jandric N, Hayes CP, Walker M, Abraamyan F, Gornik KC, Ghazani AA.
Novel RAI1:c.2736delC Variant in Smith–Magenis Syndrome: Identification by Whole Genome Sequencing and Joint Analysis. Journal of Personalized Medicine. 2024; 14(9):901.
https://doi.org/10.3390/jpm14090901
Chicago/Turabian Style
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, no. 9: 901.
https://doi.org/10.3390/jpm14090901
APA Style
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