Further evidence for distinct traits associated with RBM10 missense variants.

MLA

Poulton, Cathryn, et al. “Further Evidence for Distinct Traits Associated with RBM10 Missense Variants.” Clinical Genetics, vol. 102, no. 2, Aug. 2022, pp. 161–63. EBSCOhost, https://doi.org/10.1111/cge.14163.

APA

Poulton, C., Baynam, G., Pugh, K., Mason, M., Kiraly, B. C., Gration, D., Dreyer, L., Viti, L., Agostino, M., & Heng, J. I. (2022). Further evidence for distinct traits associated with RBM10 missense variants. Clinical Genetics, 102(2), 161–163. https://doi.org/10.1111/cge.14163

Chicago

Poulton, Cathryn, Gareth Baynam, Kye Pugh, Michael Mason, Borri, Catherine Kiraly, Dylan Gration, Lauren Dreyer, Leon Viti, Mark Agostino, and Julian Ik‐Tsen Heng. 2022. “Further Evidence for Distinct Traits Associated with RBM10 Missense Variants.” Clinical Genetics 102 (2): 161–63. doi:10.1111/cge.14163.