APA (7th ed.) Citation

H, Y., H, T., N, T., R, I., Y, T., KJ, P., . . . I, K. (2022). Family with congenital contractural arachnodactyly due to a novel multiexon deletion of the FBN2 gene. Clinical case reports, 10(2), e05335. https://doi.org/10.1002/ccr3.5335

Chicago Style (17th ed.) Citation

H, Yagi, et al. "Family with Congenital Contractural Arachnodactyly Due to a Novel Multiexon Deletion of the FBN2 Gene." Clinical Case Reports 10, no. 2 (2022): e05335. https://doi.org/10.1002/ccr3.5335.

MLA (9th ed.) Citation

H, Yagi, et al. "Family with Congenital Contractural Arachnodactyly Due to a Novel Multiexon Deletion of the FBN2 Gene." Clinical Case Reports, vol. 10, no. 2, 2022, p. e05335, https://doi.org/10.1002/ccr3.5335.