Rare and de novo coding variants in chromodomain genes in Chiari I malformation

MLA

Karen Soldano, et al. Rare and de Novo Coding Variants in Chromodomain Genes in Chiari I Malformation. Dec. 2020. 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=edsair&AN=edsair.doi.dedup.....95ac6d2e60064bcaddc86c2e83424d58&authtype=sso&custid=ns315887.

APA

Karen Soldano, Timothy Kuensting, David D. Limbrick, Brooke Sadler, Melanie E. Garrett, Alfons Macaya, Gabe Haller, Andrew T. Hale, Marco Tartaglia, Jackson Wilborn, Stephen R Gannon, Aintzane Urbizu, Giuseppe Zampino, Donald F. Conrad, Norine Voisin, Tychele N. Turner, Gerarda Cappuccio, Nicola Brunetti-Pierri, Kevin McCall, … Christina A. Gurnett. (2020). Rare and de novo coding variants in chromodomain genes in Chiari I malformation.

Chicago

Karen Soldano, Timothy Kuensting, David D. Limbrick, Brooke Sadler, Melanie E. Garrett, Alfons Macaya, Gabe Haller, et al. 2020. “Rare and de Novo Coding Variants in Chromodomain Genes in Chiari I Malformation,” December. 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=edsair&AN=edsair.doi.dedup.....95ac6d2e60064bcaddc86c2e83424d58&authtype=sso&custid=ns315887.