Identification of skewed X chromosome inactivation using exome and transcriptome sequencing in patients with suspected rare genetic disease

MLA

Numrah Fadra, 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, Apr. 2024, pp. 1–16. EBSCOhost, https://doi.org/10.1186/s12864-024-10240-2.

APA

Numrah Fadra, Laura E Schultz-Rogers, Pritha Chanana, Margot A Cousin, Erica L Macke, Alejandro Ferrer, Filippo Pinto e Vairo, Rory J Olson, Gavin R Oliver, Lindsay A Mulvihill, Garrett Jenkinson, & Eric W Klee. (2024). Identification of skewed X chromosome inactivation using exome and transcriptome sequencing in patients with suspected rare genetic disease. BMC Genomics, 25(1), 1–16. https://doi.org/10.1186/s12864-024-10240-2

Chicago

Numrah Fadra, Laura E Schultz-Rogers, Pritha Chanana, Margot A Cousin, Erica L Macke, Alejandro Ferrer, Filippo Pinto e Vairo, et al. 2024. “Identification of Skewed X Chromosome Inactivation Using Exome and Transcriptome Sequencing in Patients with Suspected Rare Genetic Disease.” BMC Genomics 25 (1): 1–16. doi:10.1186/s12864-024-10240-2.