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Dong-Yi Han

Showing results (81-90 of 96) with videos related to

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Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|December 7, 2007
[Prenatal diagnosis for hereditary deaf families assisted by genetic testing]Bing Han, Pu Dai, Qing-wei Qi, et al.
International Journal of Pediatric Otorhinolaryngology|February 19, 2011
Newborn hearing concurrent gene screening can improve care for hearing loss: a study on 14,913 Chinese newbornsQiu-Ju Wang, Ya-Li Zhao, Shao-Qi Rao, et al.
Chinese Medical Journal|January 27, 2007
Nonsense mutations in the PAX3 gene cause Waardenburg syndrome type I in two Chinese patientsShu-Zhi Yang, Ju-Yang Cao, Rui-Ning Zhang, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|September 25, 2007
[Genetic counseling and instruction for deaf couples directed by genetic testing]Bing Han, Pu Dai, Guo-jian Wang, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|July 8, 2009
Chondrocyte-specific Smad4 gene conditional knockout results in hearing loss and inner ear malformation in miceShi-ming Yang, Zhao-hui Hou, Guan Yang, et al.
Yi Chuan = Hereditas|December 2, 2006
[Mapping of gene underlying autosomal dominant non-syndromic hearing loss(DFNA)]Han-Jun Sun, Ran Tao, Jing Cheng, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|August 23, 2008
[Correlation between phonetically balanced maximum and pure tone auditory threshold among 106 auditory neuropathy patients]Lan Lan, Dong-Yi Han, Wei Shi, et al.
Developmental Neurobiology|December 11, 2008
Smad5 haploinsufficiency leads to hair cell and hearing lossShi-Ming Yang, Wei-Wei Guo, Yin-Yan Hu, et al.
Zhonghua Yi Xue Za Zhi|January 3, 2008
[Mutation of GJB2 gene in nonsyndromic hearing impairment patients: analysis of 1190 cases]Fei Yu, Dong-yi Han, Pu Dai, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|October 20, 2007
[Audiological and vestibular evaluation of new coagulation factor C homology mutation carriers in a Chinese family]Qing Sun, Su-jiang Xie, Lei Feng, et al.
Pageof 10

Showing results (81-90 of 96) with videos related to

Sort By:
Pageof 10
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|December 7, 2007
[Prenatal diagnosis for hereditary deaf families assisted by genetic testing]Bing Han, Pu Dai, Qing-wei Qi, et al.
International Journal of Pediatric Otorhinolaryngology|February 19, 2011
Newborn hearing concurrent gene screening can improve care for hearing loss: a study on 14,913 Chinese newbornsQiu-Ju Wang, Ya-Li Zhao, Shao-Qi Rao, et al.
Chinese Medical Journal|January 27, 2007
Nonsense mutations in the PAX3 gene cause Waardenburg syndrome type I in two Chinese patientsShu-Zhi Yang, Ju-Yang Cao, Rui-Ning Zhang, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|September 25, 2007
[Genetic counseling and instruction for deaf couples directed by genetic testing]Bing Han, Pu Dai, Guo-jian Wang, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|July 8, 2009
Chondrocyte-specific Smad4 gene conditional knockout results in hearing loss and inner ear malformation in miceShi-ming Yang, Zhao-hui Hou, Guan Yang, et al.
Yi Chuan = Hereditas|December 2, 2006
[Mapping of gene underlying autosomal dominant non-syndromic hearing loss(DFNA)]Han-Jun Sun, Ran Tao, Jing Cheng, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|August 23, 2008
[Correlation between phonetically balanced maximum and pure tone auditory threshold among 106 auditory neuropathy patients]Lan Lan, Dong-Yi Han, Wei Shi, et al.
Developmental Neurobiology|December 11, 2008
Smad5 haploinsufficiency leads to hair cell and hearing lossShi-Ming Yang, Wei-Wei Guo, Yin-Yan Hu, et al.
Zhonghua Yi Xue Za Zhi|January 3, 2008
[Mutation of GJB2 gene in nonsyndromic hearing impairment patients: analysis of 1190 cases]Fei Yu, Dong-yi Han, Pu Dai, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|October 20, 2007
[Audiological and vestibular evaluation of new coagulation factor C homology mutation carriers in a Chinese family]Qing Sun, Su-jiang Xie, Lei Feng, et al.
Pageof 10