APA (7th ed.) Citation

Bai, Y., Sun, Y., Yu, C., Xia, Y., Wu, J., Wang, L., . . . Kong, X. (2024). Causative role of a novel intronic indel variant in FBN1 and maternal germinal mosaicism in Marfan syndrome. Orphanet Journal of Rare Diseases, 19(1), . https://doi.org/10.1186/s13023-024-03139-4

Chicago Style (17th ed.) Citation

Bai, Ying, Yue Sun, Chenguang Yu, Yanjie Xia, Jing Wu, Li Wang, Yong Gao, Xin Tu, and Xiangdong Kong. "Causative Role of a Novel Intronic Indel Variant in FBN1 and Maternal Germinal Mosaicism in Marfan Syndrome." Orphanet Journal of Rare Diseases 19, no. 1 (2024). https://doi.org/10.1186/s13023-024-03139-4.

MLA (9th ed.) Citation

Bai, Ying, et al. "Causative Role of a Novel Intronic Indel Variant in FBN1 and Maternal Germinal Mosaicism in Marfan Syndrome." Orphanet Journal of Rare Diseases, vol. 19, no. 1, 2024, https://doi.org/10.1186/s13023-024-03139-4.