APA (7th ed.) Citation

Chen, C., Chen, Y., Chern, S., Wu, P., Su, J., Chen, Y., . . . Wang, W. (2013). Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 12q (12q24.21→qter) and partial monosomy 6q (6q27→qter) associated with coarctation of the aorta, ventriculomegaly and thickened nuchal fold. Gene, 516(1), 138-142. https://doi.org/10.1016/j.gene.2012.12.051

Chicago Style (17th ed.) Citation

Chen, Chih-Ping, Yi-Yung Chen, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Yu-Ting Chen, Li-Feng Chen, and Wayseen Wang. "Prenatal Diagnosis and Molecular Cytogenetic Characterization of De Novo Partial Trisomy 12q (12q24.21→qter) and Partial Monosomy 6q (6q27→qter) Associated with Coarctation of the Aorta, Ventriculomegaly and Thickened Nuchal Fold." Gene 516, no. 1 (2013): 138-142. https://doi.org/10.1016/j.gene.2012.12.051.

MLA (9th ed.) Citation

Chen, Chih-Ping, et al. "Prenatal Diagnosis and Molecular Cytogenetic Characterization of De Novo Partial Trisomy 12q (12q24.21→qter) and Partial Monosomy 6q (6q27→qter) Associated with Coarctation of the Aorta, Ventriculomegaly and Thickened Nuchal Fold." Gene, vol. 516, no. 1, 2013, pp. 138-142, https://doi.org/10.1016/j.gene.2012.12.051.