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-referens (17:e uppl.)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-referens (9:e uppl.)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.
