[Discovery of the gene defect in fragile X syndrome reveals a new mode of inheritance and improves diagnosis].

MLA

von Koskull, H., and J. Leisti. “[Discovery of the Gene Defect in Fragile X Syndrome Reveals a New Mode of Inheritance and Improves Diagnosis].” Duodecim; Laaketieteellinen Aikakauskirja, vol. 108, no. 17, 1992, pp. 1445–47. 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=cmedm&AN=1366164&authtype=sso&custid=ns315887.

APA

von Koskull, H., & Leisti, J. (1992). [Discovery of the gene defect in fragile X syndrome reveals a new mode of inheritance and improves diagnosis]. Duodecim; Laaketieteellinen Aikakauskirja, 108(17), 1445–1447.

Chicago

von Koskull, H, and J Leisti. 1992. “[Discovery of the Gene Defect in Fragile X Syndrome Reveals a New Mode of Inheritance and Improves Diagnosis].” Duodecim; Laaketieteellinen Aikakauskirja 108 (17): 1445–47. 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=cmedm&AN=1366164&authtype=sso&custid=ns315887.