Cite
Prospective mutation screening of three common deafness genes in a large Taiwanese Cohort with idiopathic bilateral sensorineural hearing impairment reveals a difference in the results between families from hospitals and those from rehabilitation facilities.
MLA
Wu CC, et al. “Prospective Mutation Screening of Three Common Deafness Genes in a Large Taiwanese Cohort with Idiopathic Bilateral Sensorineural Hearing Impairment Reveals a Difference in the Results between Families from Hospitals and Those from Rehabilitation Facilities.” Audiology & Neurotology, vol. 13, no. 3, May 2008, pp. 172–81. 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=asx&AN=105797449&authtype=sso&custid=ns315887.
APA
Wu CC, Chen PJ, Chiu YH, Lu YC, Wu MC, Hsu CJ, Wu, C.-C., Chen, P.-J., Chiu, Y.-H., Lu, Y.-C., Wu, M.-C., & Hsu, C.-J. (2008). Prospective mutation screening of three common deafness genes in a large Taiwanese Cohort with idiopathic bilateral sensorineural hearing impairment reveals a difference in the results between families from hospitals and those from rehabilitation facilities. Audiology & Neurotology, 13(3), 172–181.
Chicago
Wu CC, Chen PJ, Chiu YH, Lu YC, Wu MC, Hsu CJ, Chen-Chi Wu, et al. 2008. “Prospective Mutation Screening of Three Common Deafness Genes in a Large Taiwanese Cohort with Idiopathic Bilateral Sensorineural Hearing Impairment Reveals a Difference in the Results between Families from Hospitals and Those from Rehabilitation Facilities.” Audiology & Neurotology 13 (3): 172–81. 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=asx&AN=105797449&authtype=sso&custid=ns315887.