Investigation of a Novel Mouse Model of Prader-Willi Syndrome with Invalidation of Necdin and Magel2.

MLA

“Investigation of a Novel Mouse Model of Prader-Willi Syndrome with Invalidation of Necdin and Magel2.” Genomics & Genetics Weekly, Aug. 2024, p. 669. 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=edo&AN=178763282&authtype=sso&custid=ns315887.

APA

Investigation of a Novel Mouse Model of Prader-Willi Syndrome with Invalidation of Necdin and Magel2. (2024). Genomics & Genetics Weekly, 669.

Chicago

“Investigation of a Novel Mouse Model of Prader-Willi Syndrome with Invalidation of Necdin and Magel2.” 2024. Genomics & Genetics Weekly, August, 669. 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=edo&AN=178763282&authtype=sso&custid=ns315887.