Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Bulletin of the World Health Organization|October 29, 2019
Training for hearing care providersMahmood F Bhutta, Xingkuan Bu, Patricia Castellanos de Muñoz, et al.
ORL; Journal for Oto-Rhino-Laryngology and Its Related Specialties|December 15, 2006
Clinical and genetic features in a Chinese pedigree with autosomal dominant auditory neuropathyGuangqian Xing, Xin Cao, Huiqin Tian, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|January 24, 2009
[Sequence analysis of DFNB59 gene in a Chinese family with dominantly inherited auditory neuropathy]Shuai Xu, Zhibin Chen, Yajie Lu, et al.
Journal of Biomedical Research|April 5, 2013
Molecular screening of patients with nonsyndromic hearing loss from Nanjing city of ChinaYajie Lu, Dachun Dai, Zhibin Chen, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|November 27, 2007
[Sequence analysis of OTOF gene in a Chinese pedigree with autosomal dominant auditory neuropathy]Shuai Xu, Guangqian Xing, Xin Cao, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|March 19, 2010
[The application of improved CHQS for mass epidemiology study on hearing impairment]Cheng Liu, Guangqian Xing, Xia Xu, et al.
Biochemical and Biophysical Research Communications|June 20, 2006
Mitochondrial 12S rRNA A827G mutation is involved in the genetic susceptibility to aminoglycoside ototoxicityGuangqian Xing, Zhibin Chen, Qinjun Wei, et al.
American Journal of Medical Genetics. Part A|December 31, 2003
Cosegregation of C-insertion at position 961 with the A1555G mutation of the mitochondrial 12S rRNA gene in a large Chinese family with maternally inherited hearing lossRonghua Li, Guangqian Xing, Ming Yan, et al.
Biochemical and Biophysical Research Communications|May 3, 2006
Maternally inherited non-syndromic hearing loss associated with mitochondrial 12S rRNA A827G mutation in a Chinese familyGuangqian Xing, Zhibin Chen, Qinjun Wei, et al.
International Journal of Audiology|December 15, 2012
Maternally transmitted aminoglycoside-induced and non-syndromic hearing loss caused by the 1494C > T mutation in the mitochondrial 12S rRNA gene in two Chinese familiesQinjun Wei, Dan Xu, Zhibin Chen, et al.
Pageof 2