Intermittent PTH (1-34) injection rescues the retarded skeletal development and postnatal lethality of mice mimicking human achondroplasia and thanatophoric dysplasia.

MLA

Xie, Yangli, et al. “Intermittent PTH (1-34) Injection Rescues the Retarded Skeletal Development and Postnatal Lethality of Mice Mimicking Human Achondroplasia and Thanatophoric Dysplasia.” Human Molecular Genetics, vol. 21, no. 18, Sept. 2012, pp. 3941–55. EBSCOhost, https://doi.org/10.1093/hmg/dds181.

APA

Xie, Y., Su, N., Jin, M., Qi, H., Yang, J., Li, C., Du, X., Luo, F., Chen, B., Shen, Y., Huang, H., Xian, C. J., Deng, C., & Chen, L. (2012). Intermittent PTH (1-34) injection rescues the retarded skeletal development and postnatal lethality of mice mimicking human achondroplasia and thanatophoric dysplasia. Human Molecular Genetics, 21(18), 3941–3955. https://doi.org/10.1093/hmg/dds181

Chicago

Xie, Yangli, Nan Su, Min Jin, Huabing Qi, Junbao Yang, Can Li, Xiaolan Du, et al. 2012. “Intermittent PTH (1-34) Injection Rescues the Retarded Skeletal Development and Postnatal Lethality of Mice Mimicking Human Achondroplasia and Thanatophoric Dysplasia.” Human Molecular Genetics 21 (18): 3941–55. doi:10.1093/hmg/dds181.