Cite
A PTPN11 allele encoding a catalytically impaired SHP2 protein in a patient with a Noonan syndrome phenotype
MLA
Lisa Edelmann, et al. A PTPN11 Allele Encoding a Catalytically Impaired SHP2 Protein in a Patient with a Noonan Syndrome Phenotype. May 2014. 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.....b6728850dc2014bb46ffa84613368f56&authtype=sso&custid=ns315887.
APA
Lisa Edelmann, Ivan F M Lo, Bruce D. Gelb, Simone Martinelli, Jonathan J. Edwards, Lisong Shi, Luca Pannone, Marco Tartaglia, & Ho Ming Luk. (2014). A PTPN11 allele encoding a catalytically impaired SHP2 protein in a patient with a Noonan syndrome phenotype.
Chicago
Lisa Edelmann, Ivan F M Lo, Bruce D. Gelb, Simone Martinelli, Jonathan J. Edwards, Lisong Shi, Luca Pannone, Marco Tartaglia, and Ho Ming Luk. 2014. “A PTPN11 Allele Encoding a Catalytically Impaired SHP2 Protein in a Patient with a Noonan Syndrome Phenotype,” May. 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.....b6728850dc2014bb46ffa84613368f56&authtype=sso&custid=ns315887.