Cite
Accelerating novel candidate gene discovery in neurogenetic disorders via whole-exome sequencing of prescreened multiplex consanguineous families
MLA
Mohamad-Hani Temsah, et al. “Accelerating Novel Candidate Gene Discovery in Neurogenetic Disorders via Whole-Exome Sequencing of Prescreened Multiplex Consanguineous Families.” Cell Reports, vol. 10, no. 2, Aug. 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.....f59371ca100ab5709d706db11a4de0ae&authtype=sso&custid=ns315887.
APA
Mohamad-Hani Temsah, Rakad Hammami, Mohammed A. Aldahmesh, Ghada M H Abdel-Salam, Sameera Sogaty, Brian F. Meyer, Fatema Alzahrani, Mohammed Al-Owain, Hadia Hijazi, Yong Xiong, Banan Al-Younes, Mohammad Alsogheer, Fahad A. Bashiri, Amal Alhashem, Abdulrahman A. Aldeeri, Heba Y. El Khashab, Nouriya Al-Sannaa, Mais Hashem, Maha Tulbah, … Nisha Patel. (2014). Accelerating novel candidate gene discovery in neurogenetic disorders via whole-exome sequencing of prescreened multiplex consanguineous families. Cell Reports, 10(2).
Chicago
Mohamad-Hani Temsah, Rakad Hammami, Mohammed A. Aldahmesh, Ghada M H Abdel-Salam, Sameera Sogaty, Brian F. Meyer, Fatema Alzahrani, et al. 2014. “Accelerating Novel Candidate Gene Discovery in Neurogenetic Disorders via Whole-Exome Sequencing of Prescreened Multiplex Consanguineous Families.” Cell Reports 10 (2). 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.....f59371ca100ab5709d706db11a4de0ae&authtype=sso&custid=ns315887.