APA

Jiang L., Liang X., Li Y., Wang J., Zaneveld J. E., Wang H., Xu S., Wang K., Wang B., Chen R. & Sui R. (20160425). Comprehensive molecular diagnosis of 67 Chinese Usher syndrome probands: high rate of ethnicity specific mutations in Chinese USH patients. : Orphanet journal of rare diseases.

Chicago

Jiang Lichun, Liang Xiaofang, Li Yumei, Wang Jing, Zaneveld Jacques Eric, Wang Hui, Xu Shan, Wang Keqing, Wang Binbin, Chen Rui and Sui Ruifang. 20160425. Comprehensive molecular diagnosis of 67 Chinese Usher syndrome probands: high rate of ethnicity specific mutations in Chinese USH patients. : Orphanet journal of rare diseases.

Harvard

Jiang L., Liang X., Li Y., Wang J., Zaneveld J. E., Wang H., Xu S., Wang K., Wang B., Chen R. and Sui R. (20160425). Comprehensive molecular diagnosis of 67 Chinese Usher syndrome probands: high rate of ethnicity specific mutations in Chinese USH patients. : Orphanet journal of rare diseases.

MLA

Jiang Lichun, Liang Xiaofang, Li Yumei, Wang Jing, Zaneveld Jacques Eric, Wang Hui, Xu Shan, Wang Keqing, Wang Binbin, Chen Rui and Sui Ruifang. Comprehensive molecular diagnosis of 67 Chinese Usher syndrome probands: high rate of ethnicity specific mutations in Chinese USH patients. : Orphanet journal of rare diseases. 20160425.