A novel Xp22.11 deletion causing a syndrome of craniosynostosis and periventricular nodular heterotopia.

MLA

van Kogelenberg, Margriet, et al. “A Novel Xp22.11 Deletion Causing a Syndrome of Craniosynostosis and Periventricular Nodular Heterotopia.” American Journal of Medical Genetics. Part A, vol. 155A, no. 12, Dec. 2011, pp. 3144–47. EBSCOhost, https://doi.org/10.1002/ajmg.a.34311.

APA

van Kogelenberg, M., Lerone, M., De Toni, T., Divizia, M. T., de Brouwer, A. P. M., Veltman, J. A., van Bokhoven, H., & Robertson, S. P. (2011). A novel Xp22.11 deletion causing a syndrome of craniosynostosis and periventricular nodular heterotopia. American Journal of Medical Genetics. Part A, 155A(12), 3144–3147. https://doi.org/10.1002/ajmg.a.34311

Chicago

van Kogelenberg, Margriet, Margherita Lerone, Teresa De Toni, Maria T. Divizia, Arjan P.M. de Brouwer, Joris A. Veltman, Hans van Bokhoven, and Stephen P. Robertson. 2011. “A Novel Xp22.11 Deletion Causing a Syndrome of Craniosynostosis and Periventricular Nodular Heterotopia.” American Journal of Medical Genetics. Part A 155A (12): 3144–47. doi:10.1002/ajmg.a.34311.