Personal utility of genomic sequencing for infants with congenital deafness

MLA

Tutty, E., et al. Personal Utility of Genomic Sequencing for Infants with Congenital Deafness. 2021. 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.on1315692940&authtype=sso&custid=ns315887.

APA

Tutty, E., Amor, D., Jarmolowicz, A., Paton, K., & Downie, L. (2021). Personal utility of genomic sequencing for infants with congenital deafness.

Chicago

Tutty, E, Dj Amor, A Jarmolowicz, K Paton, and L Downie. 2021. “Personal Utility of Genomic Sequencing for Infants with Congenital Deafness.” 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.on1315692940&authtype=sso&custid=ns315887.