Cite
Analysis of Hungarian patients with Rett syndrome phenotype for MECP2, CDKL5 and FOXG1 gene mutations.
MLA
Hadzsiev, Kinga, et al. “Analysis of Hungarian Patients with Rett Syndrome Phenotype for MECP2, CDKL5 and FOXG1 Gene Mutations.” Journal of Human Genetics, vol. 56, no. 3, Mar. 2011, pp. 183–87. EBSCOhost, https://doi.org/10.1038/jhg.2010.156.
APA
Hadzsiev, K., Polgar, N., Bene, J., Komlosi, K., Karteszi, J., Hollody, K., Kosztolanyi, G., Renieri, A., & Melegh, B. (2011). Analysis of Hungarian patients with Rett syndrome phenotype for MECP2, CDKL5 and FOXG1 gene mutations. Journal of Human Genetics, 56(3), 183–187. https://doi.org/10.1038/jhg.2010.156
Chicago
Hadzsiev, Kinga, Noemi Polgar, Judit Bene, Katalin Komlosi, Judit Karteszi, Katalin Hollody, Gyorgy Kosztolanyi, Alessandra Renieri, and Bela Melegh. 2011. “Analysis of Hungarian Patients with Rett Syndrome Phenotype for MECP2, CDKL5 and FOXG1 Gene Mutations.” Journal of Human Genetics 56 (3): 183–87. doi:10.1038/jhg.2010.156.