PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature

MLA

Reijnders, Margot R. F., et al. “PURA Syndrome: Clinical Delineation and Genotype-Phenotype Study in 32 Individuals with Review of Published Literature.” Journal of Medical Genetics (JMG), vol. 55, no. 2, Jan. 2018, pp. 104–13. EBSCOhost, https://doi.org/10.1136/jmedgenet-2017-104946.

APA

Reijnders, M. R. F., Janowski, R., Alvi, M., Self, J. E., van Essen, T. J., Vreeburg, M., Rouhl, R. P. W., Stevens, S. J. C., Stegmann, A. P. A., Schieving, J., Pfundt, R., van Dijk, K., Smeets, E., Stumpel, C. T. R. M., Bok, L. A., Cobben, J. M., Engelen, M., Mansour, S., Whiteford, M., … Baralle, D. (2018). PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature. Journal of Medical Genetics (JMG), 55(2), 104–113. https://doi.org/10.1136/jmedgenet-2017-104946

Chicago

Reijnders, Margot R F, Robert Janowski, Mohsan Alvi, Jay E Self, Ton J van Essen, Maaike Vreeburg, Rob P W Rouhl, et al. 2018. “PURA Syndrome: Clinical Delineation and Genotype-Phenotype Study in 32 Individuals with Review of Published Literature.” Journal of Medical Genetics (JMG) 55 (2): 104–13. doi:10.1136/jmedgenet-2017-104946.