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.) CitationTA, 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.) CitationTA, 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.