APA (7th ed.) Citation

TA, M., M, A., SHUH, G., NO, C., SA, B., A, H., . . . SZT, G. (2024). A Novel Missense Variant in the CHST3 Underlies Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations. Molecular syndromology, 15(5), 355. https://doi.org/10.1159/000538039

Chicago Style (17th ed.) Citation

TA, Mughal, Asim M, Gillani SHUH, Chughtai NO, Batool SA, Hussain A, Shujaat K, and Gilani SZT. "A Novel Missense Variant in the CHST3 Underlies Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations." Molecular Syndromology 15, no. 5 (2024): 355. https://doi.org/10.1159/000538039.

MLA (9th ed.) Citation

TA, Mughal, et al. "A Novel Missense Variant in the CHST3 Underlies Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations." Molecular Syndromology, vol. 15, no. 5, 2024, p. 355, https://doi.org/10.1159/000538039.

Warning: These citations may not always be 100% accurate.