Cite
HIST1H1E heterozygous protein-truncating variants cause a recognizable syndrome with intellectual disability and distinctive facial gestalt: A study to clarify the HIST1H1E syndrome phenotype in 30 individuals
MLA
Burkardt, Dd, et al. HIST1H1E Heterozygous Protein-Truncating Variants Cause a Recognizable Syndrome with Intellectual Disability and Distinctive Facial Gestalt: A Study to Clarify the HIST1H1E Syndrome Phenotype in 30 Individuals. 2019. 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.on1315736264&authtype=sso&custid=ns315887.
APA
Burkardt, D., Zachariou, A., Loveday, C., Allen, C., Amor, D., Ardissone, A., Banka, S., Bourgois, A., Coubes, C., Cytrynbaum, C., Faivre, L., Marion, G., Horton, R., Kotzot, D., Lay-Son, G., Lees, M., Low, K., Luk, H.-M., Mark, P., … Tatton-Brown, K. (2019). HIST1H1E heterozygous protein-truncating variants cause a recognizable syndrome with intellectual disability and distinctive facial gestalt: A study to clarify the HIST1H1E syndrome phenotype in 30 individuals.
Chicago
Burkardt, Dd, A Zachariou, C Loveday, Cl Allen, Dj Amor, A Ardissone, S Banka, et al. 2019. “HIST1H1E Heterozygous Protein-Truncating Variants Cause a Recognizable Syndrome with Intellectual Disability and Distinctive Facial Gestalt: A Study to Clarify the HIST1H1E Syndrome Phenotype in 30 Individuals.” 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.on1315736264&authtype=sso&custid=ns315887.