APA (7th ed.) Citation

Fadra, N., Schultz-Rogers, L. E., Chanana, P., Cousin, M. A., Macke, E. L., Ferrer, A., . . . Klee, E. W. (2024). Identification of skewed X chromosome inactivation using exome and transcriptome sequencing in patients with suspected rare genetic disease. BMC genomics, 25(1), 371-16. https://doi.org/10.1186/s12864-024-10240-2

Chicago Style (17th ed.) Citation

Fadra, Numrah, et al. "Identification of Skewed X Chromosome Inactivation Using Exome and Transcriptome Sequencing in Patients with Suspected Rare Genetic Disease." BMC Genomics 25, no. 1 (2024): 371-16. https://doi.org/10.1186/s12864-024-10240-2.

MLA (9th ed.) Citation

Fadra, Numrah, et al. "Identification of Skewed X Chromosome Inactivation Using Exome and Transcriptome Sequencing in Patients with Suspected Rare Genetic Disease." BMC Genomics, vol. 25, no. 1, 2024, pp. 371-16, https://doi.org/10.1186/s12864-024-10240-2.