APA (7th ed.) Citation

Lao, Q., Brookner, B., & Merke, D. P. (2019). High-Throughput Screening for CYP21A1P-TNXA/TNXB Chimeric Genes Responsible for Ehlers-Danlos Syndrome in Patients with Congenital Adrenal Hyperplasia. The Journal of molecular diagnostics : JMD, 21(5), 924-931. https://doi.org/10.1016/j.jmoldx.2019.06.001

Chicago Style (17th ed.) Citation

Lao, Qizong, Brittany Brookner, and Deborah P. Merke. "High-Throughput Screening for CYP21A1P-TNXA/TNXB Chimeric Genes Responsible for Ehlers-Danlos Syndrome in Patients with Congenital Adrenal Hyperplasia." The Journal of Molecular Diagnostics : JMD 21, no. 5 (2019): 924-931. https://doi.org/10.1016/j.jmoldx.2019.06.001.

MLA (9th ed.) Citation

Lao, Qizong, et al. "High-Throughput Screening for CYP21A1P-TNXA/TNXB Chimeric Genes Responsible for Ehlers-Danlos Syndrome in Patients with Congenital Adrenal Hyperplasia." The Journal of Molecular Diagnostics : JMD, vol. 21, no. 5, 2019, pp. 924-931, https://doi.org/10.1016/j.jmoldx.2019.06.001.