Detection of a de novo Y278C mutation in FGFR3 in a pregnancy with severe fetal hypochondroplasia: Prenatal diagnosis and literature review

MLA

Jun-Wei Su, et al. “Detection of a de Novo Y278C Mutation in FGFR3 in a Pregnancy with Severe Fetal Hypochondroplasia: Prenatal Diagnosis and Literature Review.” Taiwanese Journal of Obstetrics & Gynecology, vol. 52, no. 4, Dec. 2013, pp. 580–85. 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.....7d543ee6c31157cdab36c13d3acbee6b&authtype=sso&custid=ns315887.

APA

Jun-Wei Su, Yi-Ning Su, Tzu-Hung Lin, Chih-Ping Chen, Tung-Yao Chang, & Wayseen Wang. (2013). Detection of a de novo Y278C mutation in FGFR3 in a pregnancy with severe fetal hypochondroplasia: Prenatal diagnosis and literature review. Taiwanese Journal of Obstetrics & Gynecology, 52(4), 580–585.

Chicago

Jun-Wei Su, Yi-Ning Su, Tzu-Hung Lin, Chih-Ping Chen, Tung-Yao Chang, and Wayseen Wang. 2013. “Detection of a de Novo Y278C Mutation in FGFR3 in a Pregnancy with Severe Fetal Hypochondroplasia: Prenatal Diagnosis and Literature Review.” Taiwanese Journal of Obstetrics & Gynecology 52 (4): 580–85. 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.....7d543ee6c31157cdab36c13d3acbee6b&authtype=sso&custid=ns315887.