APA (7th ed.) Citation

Wei, L., Yang, Y., Jiang, T., Zhang, C., Chen, C., Huang, M., . . . Gao, F. (2025). Different mutations in TBL1XR1 lead to diverse phenotypes of neurodevelopmental disorder: Two case reports. BMC Medical Genomics, 18(1), 1. https://doi.org/10.1186/s12920-025-02169-6

Chicago Style (17th ed.) Citation

Wei, Linlin, Yonghui Yang, Tiejia Jiang, Chaolang Zhang, Cuiying Chen, Mingwei Huang, Nannan Li, Huachun Xiong, and Feng Gao. "Different Mutations in TBL1XR1 Lead to Diverse Phenotypes of Neurodevelopmental Disorder: Two Case Reports." BMC Medical Genomics 18, no. 1 (2025): 1. https://doi.org/10.1186/s12920-025-02169-6.

MLA (9th ed.) Citation

Wei, Linlin, et al. "Different Mutations in TBL1XR1 Lead to Diverse Phenotypes of Neurodevelopmental Disorder: Two Case Reports." BMC Medical Genomics, vol. 18, no. 1, 2025, p. 1, https://doi.org/10.1186/s12920-025-02169-6.