Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Dongyi Han

Showing results (121-130 of 141) with videos related to

Pageof 15
Sort By:
Genetic Testing and Molecular Biomarkers|April 15, 2011
Phenotype-genotype correlation in 295 Chinese deaf subjects with biallelic causative mutations in the GJB2 geneFei-Fan Zhao, Yu-Bin Ji, Da-Yong Wang, et al.
Biochemical and Biophysical Research Communications|December 29, 2005
Clinical and molecular analysis of a four-generation Chinese family with aminoglycoside-induced and nonsyndromic hearing loss associated with the mitochondrial 12S rRNA C1494T mutationQiuju Wang, Qing-Zhong Li, Dongyi Han, et al.
Head & Face Medicine|July 25, 2023
Surgical management and the prognosis of iatrogenic facial nerve injury in middle ear surgery: a 20-year experienceJianbin Sun, Ruoya Wang, Xingrui Chen, et al.
Journal of Human Genetics|September 19, 2014
Resolving the genetic heterogeneity of prelingual hearing loss within one family: Performance comparison and application of two targeted next generation sequencing approachesYu Lu, Xueya Zhou, Zhanguo Jin, et al.
Lin Chuang Er Bi Yan Hou Ke Za Zhi = Journal of Clinical Otorhinolaryngology|May 23, 2006
[Genotypic analysis of familial dilated vestibular aqueduct syndrome]Pu Dai, Dongyi Han, Juyang Cao, et al.
Annals of Human Genetics|September 18, 2014
Exome sequencing identifies a novel frameshift mutation of MYO6 as the cause of autosomal dominant nonsyndromic hearing loss in a Chinese familyJing Cheng, Xueya Zhou, Yu Lu, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|March 16, 2026
Genotype-phenotype correlation-driven precision management in hereditary conductive and mixed hearing lossQin Wang, Xiedong Wu, Guojie Dong, et al.
Biochemical and Biophysical Research Communications|August 19, 2007
Coexistence of mitochondrial 12S rRNA C1494T and CO1/tRNA(Ser(UCN)) G7444A mutations in two Han Chinese pedigrees with aminoglycoside-induced and non-syndromic hearing lossHuijun Yuan, Jing Chen, Xin Liu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 17, 2007
The prevalence of the 235delC GJB2 mutation in a Chinese deaf populationPu Dai, Fei Yu, Bing Han, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|August 4, 2011
[Cochlear implantation with pericanal electrode insertion technique]Tingting Cui, Hong Jiang, Xiaowei Chen, et al.
Pageof 15

Showing results (121-130 of 141) with videos related to

Sort By:
Pageof 15
Genetic Testing and Molecular Biomarkers|April 15, 2011
Phenotype-genotype correlation in 295 Chinese deaf subjects with biallelic causative mutations in the GJB2 geneFei-Fan Zhao, Yu-Bin Ji, Da-Yong Wang, et al.
Biochemical and Biophysical Research Communications|December 29, 2005
Clinical and molecular analysis of a four-generation Chinese family with aminoglycoside-induced and nonsyndromic hearing loss associated with the mitochondrial 12S rRNA C1494T mutationQiuju Wang, Qing-Zhong Li, Dongyi Han, et al.
Head & Face Medicine|July 25, 2023
Surgical management and the prognosis of iatrogenic facial nerve injury in middle ear surgery: a 20-year experienceJianbin Sun, Ruoya Wang, Xingrui Chen, et al.
Journal of Human Genetics|September 19, 2014
Resolving the genetic heterogeneity of prelingual hearing loss within one family: Performance comparison and application of two targeted next generation sequencing approachesYu Lu, Xueya Zhou, Zhanguo Jin, et al.
Lin Chuang Er Bi Yan Hou Ke Za Zhi = Journal of Clinical Otorhinolaryngology|May 23, 2006
[Genotypic analysis of familial dilated vestibular aqueduct syndrome]Pu Dai, Dongyi Han, Juyang Cao, et al.
Annals of Human Genetics|September 18, 2014
Exome sequencing identifies a novel frameshift mutation of MYO6 as the cause of autosomal dominant nonsyndromic hearing loss in a Chinese familyJing Cheng, Xueya Zhou, Yu Lu, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|March 16, 2026
Genotype-phenotype correlation-driven precision management in hereditary conductive and mixed hearing lossQin Wang, Xiedong Wu, Guojie Dong, et al.
Biochemical and Biophysical Research Communications|August 19, 2007
Coexistence of mitochondrial 12S rRNA C1494T and CO1/tRNA(Ser(UCN)) G7444A mutations in two Han Chinese pedigrees with aminoglycoside-induced and non-syndromic hearing lossHuijun Yuan, Jing Chen, Xin Liu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 17, 2007
The prevalence of the 235delC GJB2 mutation in a Chinese deaf populationPu Dai, Fei Yu, Bing Han, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|August 4, 2011
[Cochlear implantation with pericanal electrode insertion technique]Tingting Cui, Hong Jiang, Xiaowei Chen, et al.
Pageof 15