APA (7th ed.) Citation

Q, L., A, S., S, K., S, K., D, B., A, M., . . . DP, M. (2026). Clinical and Biochemical Phenotype Across the Genotypic Spectrum of 21-hydroxylase Deficiency in 457 Individuals. The Journal of clinical endocrinology and metabolism, 111(4), 1098. https://doi.org/10.1210/clinem/dgaf546

Chicago Style (17th ed.) Citation

Q, Lao, Schulman A, Kulkarni S, Kollender S, Bick D, Moon A, Burkardt D, and Merke DP. "Clinical and Biochemical Phenotype Across the Genotypic Spectrum of 21-hydroxylase Deficiency in 457 Individuals." The Journal of Clinical Endocrinology and Metabolism 111, no. 4 (2026): 1098. https://doi.org/10.1210/clinem/dgaf546.

MLA (9th ed.) Citation

Q, Lao, et al. "Clinical and Biochemical Phenotype Across the Genotypic Spectrum of 21-hydroxylase Deficiency in 457 Individuals." The Journal of Clinical Endocrinology and Metabolism, vol. 111, no. 4, 2026, p. 1098, https://doi.org/10.1210/clinem/dgaf546.