APA (7th ed.) Citation

Hamiel, U., Kurolap, A., Chai Gadot, C., Mory, A., Bar Shira, A., Baris Feldman, H., & Marom, D. (2025). Deletion of RAI1 noncoding exons 1–2 causes Smith–Magenis syndrome: Noncoding RAI1 deletion causes Smith-Magenis syndrome: U. Hamiel et al. Journal of Genetics, 104(1), 1. https://doi.org/10.1007/s12041-025-01497-x

Chicago Style (17th ed.) Citation

Hamiel, Uri, Alina Kurolap, Chofit Chai Gadot, Adi Mory, Anat Bar Shira, Hagit Baris Feldman, and Daphna Marom. "Deletion of RAI1 Noncoding Exons 1–2 Causes Smith–Magenis Syndrome: Noncoding RAI1 Deletion Causes Smith-Magenis Syndrome: U. Hamiel Et Al." Journal of Genetics 104, no. 1 (2025): 1. https://doi.org/10.1007/s12041-025-01497-x.

MLA (9th ed.) Citation

Hamiel, Uri, et al. "Deletion of RAI1 Noncoding Exons 1–2 Causes Smith–Magenis Syndrome: Noncoding RAI1 Deletion Causes Smith-Magenis Syndrome: U. Hamiel Et Al." Journal of Genetics, vol. 104, no. 1, 2025, p. 1, https://doi.org/10.1007/s12041-025-01497-x.