APA (7th ed.) Citation

Zouaghi, Y., Choudhary, A. M., Irshad, S., Adamo, M., Rehman, K. u., Fatima, A., . . . Pitteloud, N. (2024). Genome sequencing reveals novel causative structural and single nucleotide variants in Pakistani families with congenital hypogonadotropic hypogonadism. BMC Genomics, 25(1), . https://doi.org/10.1186/s12864-024-10598-3

Chicago Style (17th ed.) Citation

Zouaghi, Yassine, et al. "Genome Sequencing Reveals Novel Causative Structural and Single Nucleotide Variants in Pakistani Families with Congenital Hypogonadotropic Hypogonadism." BMC Genomics 25, no. 1 (2024). https://doi.org/10.1186/s12864-024-10598-3.

MLA (9th ed.) Citation

Zouaghi, Yassine, et al. "Genome Sequencing Reveals Novel Causative Structural and Single Nucleotide Variants in Pakistani Families with Congenital Hypogonadotropic Hypogonadism." BMC Genomics, vol. 25, no. 1, 2024, https://doi.org/10.1186/s12864-024-10598-3.