Cite
PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature
MLA
Reijnders, M. R. F., et al. “PURA Syndrome: Clinical Delineation and Genotype-Phenotype Study in 32 Individuals with Review of Published Literature.” Journal of Medical Genetics, 2018. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsoai&AN=edsoai.on1283997419&authtype=sso&custid=ns315887.
APA
Reijnders, M. R. F., Janowski, R., Alvi, M., Self, J. E., Essen, T. J. van, Vreeburg, M., Rouhl, R. P. W., Stevens, S. J. C., Stegmann, A. P. A., Schieving, J. H., Pfundt, R. P., Dijk, K. van, Smeets, E., Stumpel, C., Bok, L. ., 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.
Chicago
Reijnders, M.R.F., R. Janowski, M. Alvi, J.E. Self, T.J. van Essen, M. Vreeburg, R.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. http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsoai&AN=edsoai.on1283997419&authtype=sso&custid=ns315887.