De novo microduplications at 1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL association.

MLA

Hilger, Alina, et al. “De Novo Microduplications at 1q41, 2q37.3, and 8q24.3 in Patients with VATER/VACTERL Association.” European Journal of Human Genetics : EJHG, vol. 21, no. 12, Dec. 2013, pp. 1377–82. EBSCOhost, https://doi.org/10.1038/ejhg.2013.58.

APA

Hilger, A., Schramm, C., Pennimpede, T., Wittler, L., Dworschak, G. C., Bartels, E., Engels, H., Zink, A. M., Degenhardt, F., Müller, A. M., Schmiedeke, E., Grasshoff-Derr, S., Märzheuser, S., Hosie, S., Holland-Cunz, S., Wijers, C. H. W., Marcelis, C. L. M., van Rooij, I. A. L. M., Hildebrandt, F., … Draaken, M. (2013). De novo microduplications at 1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL association. European Journal of Human Genetics : EJHG, 21(12), 1377–1382. https://doi.org/10.1038/ejhg.2013.58

Chicago

Hilger, Alina, Charlotte Schramm, Tracie Pennimpede, Lars Wittler, Gabriel C Dworschak, Enrika Bartels, Hartmut Engels, et al. 2013. “De Novo Microduplications at 1q41, 2q37.3, and 8q24.3 in Patients with VATER/VACTERL Association.” European Journal of Human Genetics : EJHG 21 (12): 1377–82. doi:10.1038/ejhg.2013.58.