APA (7th ed.) Citation

Arefzadeh, M., Rabbani, B., Abdolahpour, S., Emami, F., Abbasi, F., Masoumi, T., . . . Mahdieh, N. (2026). A Novel Homozygous CUL7 Variant in an Iranian Patient Expands the Genetic Spectrum of 3 M Syndrome. Clinical Case Reports, 14(3), 1. https://doi.org/10.1002/ccr3.72218

Chicago Style (17th ed.) Citation

Arefzadeh, Maryam, Bahareh Rabbani, Saeideh Abdolahpour, Farnoosh Emami, Farzaneh Abbasi, Tannaz Masoumi, Siamak Mirab Samiee, Ali Rabbani, and Nejat Mahdieh. "A Novel Homozygous CUL7 Variant in an Iranian Patient Expands the Genetic Spectrum of 3 M Syndrome." Clinical Case Reports 14, no. 3 (2026): 1. https://doi.org/10.1002/ccr3.72218.

MLA (9th ed.) Citation

Arefzadeh, Maryam, et al. "A Novel Homozygous CUL7 Variant in an Iranian Patient Expands the Genetic Spectrum of 3 M Syndrome." Clinical Case Reports, vol. 14, no. 3, 2026, p. 1, https://doi.org/10.1002/ccr3.72218.