Utility of whole-genome sequencing for detection of newborn screening disorders in a population cohort of 1,696 neonates

MLA

Elisabeth Klein, et al. “Utility of Whole-Genome Sequencing for Detection of Newborn Screening Disorders in a Population Cohort of 1,696 Neonates.” Genetics in Medicine : Official Journal of the American College of Medical Genetics, vol. 18, no. 3, May 2015. 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.....62ea57b3140475c9e4cffb35fb08e598&authtype=sso&custid=ns315887.

APA

Elisabeth Klein, Prachi Kothiyal, Benjamin D. Solomon, Joseph G. Vockley, Irina Remsburg, Daniel Stauffer, Ramaswamy K. Iyer, Kathi Huddleston, George L. Maxwell, Dale L. Bodian, John E. Niederhuber, Wendy S.W. Wong, Alina Khromykh, Robin Baker, & Amber D. Gaither. (2015). Utility of whole-genome sequencing for detection of newborn screening disorders in a population cohort of 1,696 neonates. Genetics in Medicine : Official Journal of the American College of Medical Genetics, 18(3).

Chicago

Elisabeth Klein, Prachi Kothiyal, Benjamin D. Solomon, Joseph G. Vockley, Irina Remsburg, Daniel Stauffer, Ramaswamy K. Iyer, et al. 2015. “Utility of Whole-Genome Sequencing for Detection of Newborn Screening Disorders in a Population Cohort of 1,696 Neonates.” Genetics in Medicine : Official Journal of the American College of Medical Genetics 18 (3). 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.....62ea57b3140475c9e4cffb35fb08e598&authtype=sso&custid=ns315887.