Cite
DFNA49, a novel locus for autosomal dominant non-syndromic hearing loss, maps proximal to DFNA7/DFNM1 region on chromosome 1q21-q23
MLA
Silvia Modamio-Høybjør, et al. “DFNA49, a Novel Locus for Autosomal Dominant Non-Syndromic Hearing Loss, Maps Proximal to DFNA7/DFNM1 Region on Chromosome 1q21-Q23.” Journal of Medical Genetics, vol. 40, no. 11, Nov. 2003. 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.....3c9fa1befdb4529032ff1c8832a45c8e&authtype=sso&custid=ns315887.
APA
Silvia Modamio-Høybjør, I del Castillo, M A Moreno-Pelayo, Ángeles Mencía, Miguel Fernández-Burriel, F Moreno, Christine Petit, Sébastien Chardenoux, & Mark Lathrop. (2003). DFNA49, a novel locus for autosomal dominant non-syndromic hearing loss, maps proximal to DFNA7/DFNM1 region on chromosome 1q21-q23. Journal of Medical Genetics, 40(11).
Chicago
Silvia Modamio-Høybjør, I del Castillo, M A Moreno-Pelayo, Ángeles Mencía, Miguel Fernández-Burriel, F Moreno, Christine Petit, Sébastien Chardenoux, and Mark Lathrop. 2003. “DFNA49, a Novel Locus for Autosomal Dominant Non-Syndromic Hearing Loss, Maps Proximal to DFNA7/DFNM1 Region on Chromosome 1q21-Q23.” Journal of Medical Genetics 40 (11). 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.....3c9fa1befdb4529032ff1c8832a45c8e&authtype=sso&custid=ns315887.