APA (7th ed.) Citation

SB, L., CY, C., YR, C., YJ, C., CF, Y., YH, L., & DM, N. (2026). Genotype-phenotype correlation of biallelic DUOX2 mutations in transient and permanent congenital hypothyroidism. Journal of the Endocrine Society, 10(6), bvag081. https://doi.org/10.1210/jendso/bvag081

Chicago Style (17th ed.) Citation

SB, Liang, Cheng CY, Chen YR, Chen YJ, Yang CF, Lu YH, and Niu DM. "Genotype-phenotype Correlation of Biallelic DUOX2 Mutations in Transient and Permanent Congenital Hypothyroidism." Journal of the Endocrine Society 10, no. 6 (2026): bvag081. https://doi.org/10.1210/jendso/bvag081.

MLA (9th ed.) Citation

SB, Liang, et al. "Genotype-phenotype Correlation of Biallelic DUOX2 Mutations in Transient and Permanent Congenital Hypothyroidism." Journal of the Endocrine Society, vol. 10, no. 6, 2026, p. bvag081, https://doi.org/10.1210/jendso/bvag081.