Heterozygous FGF8 mutations in patients presenting cryptorchidism and multiple VATER/VACTERL features without limb anomalies.

MLA

Zeidler, Claudia, et al. “Heterozygous FGF8 Mutations in Patients Presenting Cryptorchidism and Multiple VATER/VACTERL Features without Limb Anomalies.” Birth Defects Research. Part A: Clinical & Molecular Teratology, vol. 100, no. 10, Oct. 2014, pp. 750–59. EBSCOhost, https://doi.org/10.1002/bdra.23278.

APA

Zeidler, C., Woelfle, J., Draaken, M., Mughal, S. S., Große, G., Hilger, A. C., Dworschak, G. C., Boemers, T. M., Jenetzky, E., Zwink, N., Lacher, M., Schmidt, D., Schmiedeke, E., Grasshoff, D. S., Märzheuser, S., Holland, C. S., Schäfer, M., Bartels, E., Keppler, K., & Palta, M. (2014). Heterozygous FGF8 mutations in patients presenting cryptorchidism and multiple VATER/VACTERL features without limb anomalies. Birth Defects Research. Part A: Clinical & Molecular Teratology, 100(10), 750–759. https://doi.org/10.1002/bdra.23278

Chicago

Zeidler, Claudia, Joachim Woelfle, Markus Draaken, Sadaf S. Mughal, Greta Große, Alina C. Hilger, Gabriel C. Dworschak, et al. 2014. “Heterozygous FGF8 Mutations in Patients Presenting Cryptorchidism and Multiple VATER/VACTERL Features without Limb Anomalies.” Birth Defects Research. Part A: Clinical & Molecular Teratology 100 (10): 750–59. doi:10.1002/bdra.23278.