Cite
FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis.
MLA
Radha Rama Devi, Akella, et al. “FOXN1 Italian Founder Mutation in Indian Family: Implications in Prenatal Diagnosis.” Gene, vol. 627, Sept. 2017, pp. 222–25. EBSCOhost, https://doi.org/10.1016/j.gene.2017.06.033.
APA
Radha Rama Devi, A., Panday, N. N., & Naushad, S. M. (2017). FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis. Gene, 627, 222–225. https://doi.org/10.1016/j.gene.2017.06.033
Chicago
Radha Rama Devi, Akella, Nagesh Narayan Panday, and Shaik Mohammad Naushad. 2017. “FOXN1 Italian Founder Mutation in Indian Family: Implications in Prenatal Diagnosis.” Gene 627 (September): 222–25. doi:10.1016/j.gene.2017.06.033.