Cite
Microdeletions including FMR1 in three female patients with intellectual disability - further delineation of the phenotype and expression studies.
MLA
Zink, A. M., et al. “Microdeletions Including FMR1 in Three Female Patients with Intellectual Disability - Further Delineation of the Phenotype and Expression Studies.” Molecular Syndromology, vol. 5, no. 2, Feb. 2014, pp. 65–75. EBSCOhost, https://doi.org/10.1159/000357962.
APA
Zink, A. M., Wohlleber, E., Engels, H., Rødningen, O. K., Ravn, K., Heilmann, S., Rehnitz, J., Katzorke, N., Kraus, C., Blichfeldt, S., Hoffmann, P., Reutter, H., Brockschmidt, F. F., Kreiß-Nachtsheim, M., Vogt, P. H., Prescott, T. E., Tümer, Z., & Lee, J. A. (2014). Microdeletions including FMR1 in three female patients with intellectual disability - further delineation of the phenotype and expression studies. Molecular Syndromology, 5(2), 65–75. https://doi.org/10.1159/000357962
Chicago
Zink, A M, E Wohlleber, H Engels, O K Rødningen, K Ravn, S Heilmann, J Rehnitz, et al. 2014. “Microdeletions Including FMR1 in Three Female Patients with Intellectual Disability - Further Delineation of the Phenotype and Expression Studies.” Molecular Syndromology 5 (2): 65–75. doi:10.1159/000357962.