Yamoto, K., Saitsu, H., Fujisawa, Y., Kato, F., Matsubara, K., Fukami, M., . . . Ogata, T. (2020). Coffin‐Lowry syndrome in a girl with 46,XX,t(X;11)(p22;p15)dn: Identification of RPS6KA3 disruption by whole genome sequencing. Clin Case Rep.
Citação norma ChicagoYamoto, Kaori, Hirotomo Saitsu, Yasuko Fujisawa, Fumiko Kato, Keiko Matsubara, Maki Fukami, Masayo Kagami, and Tsutomu Ogata. "Coffin‐Lowry Syndrome in a Girl With 46,XX,t(X;11)(p22;p15)dn: Identification of RPS6KA3 Disruption By Whole Genome Sequencing." Clin Case Rep 2020.
Citação norma MLAYamoto, Kaori, et al. "Coffin‐Lowry Syndrome in a Girl With 46,XX,t(X;11)(p22;p15)dn: Identification of RPS6KA3 Disruption By Whole Genome Sequencing." Clin Case Rep 2020.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.