Cite
Mutations in the RSK2(RPS6KA3) gene cause Coffin-Lowry syndrome and nonsyndromic X-linked mental retardation
MLA
Ying Luo, et al. “Mutations in the RSK2(RPS6KA3) Gene Cause Coffin-Lowry Syndrome and Nonsyndromic X-Linked Mental Retardation.” Clinical Genetics, vol. 70, no. 6, Nov. 2006. 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.....aade639a8c94c35cd649f9a5aa940623&authtype=sso&custid=ns315887.
APA
Ying Luo, Jon W. Teague, Michael Field, Michael R. Stratton, Jackie Boyle, Gillian Turner, F L Raymond, Sarah Edkins, J Goodship, Richard Wooster, Patrick S. Tarpey, Jenny Moon, & P A Futreal. (2006). Mutations in the RSK2(RPS6KA3) gene cause Coffin-Lowry syndrome and nonsyndromic X-linked mental retardation. Clinical Genetics, 70(6).
Chicago
Ying Luo, Jon W. Teague, Michael Field, Michael R. Stratton, Jackie Boyle, Gillian Turner, F L Raymond, et al. 2006. “Mutations in the RSK2(RPS6KA3) Gene Cause Coffin-Lowry Syndrome and Nonsyndromic X-Linked Mental Retardation.” Clinical Genetics 70 (6). 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.....aade639a8c94c35cd649f9a5aa940623&authtype=sso&custid=ns315887.