Identification of an IGF1 mutation (c.15+3G>A) in familial osteonecrosis of the femoral head: A case report.

MLA

Xu, Qi, et al. “Identification of an IGF1 Mutation (c.15+3G>A) in Familial Osteonecrosis of the Femoral Head: A Case Report.” Medicine, vol. 100, no. 1, Jan. 2021, p. e23705. EBSCOhost, https://doi.org/10.1097/MD.0000000000023705.

APA

Xu, Q., Song, D., Wu, Z., Fu, B., Zheng, J., Li, R., Yin, H., Chen, S., & Wang, D. (2021). Identification of an IGF1 mutation (c.15+3G>A) in familial osteonecrosis of the femoral head: A case report. Medicine, 100(1), e23705. https://doi.org/10.1097/MD.0000000000023705

Chicago

Xu, Qi, Da Song, Zhensong Wu, Bo Fu, Juan Zheng, Rongrong Li, Han Yin, Shuangfeng Chen, and Dawei Wang. 2021. “Identification of an IGF1 Mutation (c.15+3G>A) in Familial Osteonecrosis of the Femoral Head: A Case Report.” Medicine 100 (1): e23705. doi:10.1097/MD.0000000000023705.