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Pu Dai

Showing results (191-200 of 218) with videos related to

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Journal of Human Genetics|December 15, 2010
Novel missense mutations in MYO7A underlying postlingual high- or low-frequency non-syndromic hearing impairment in two large families from ChinaYi Sun, Jing Chen, Hanjun Sun, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|September 30, 2006
[Patients suffered from enlarged vestibular aqueduct syndrome in Chifeng deaf and dumb school detected by Pendred's syndrome gene hot spot mutation screening]Pu Dai, Xiu-Hui Zhu, Yong-Yi Yuan, 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.
Medicine|February 17, 2023
Cochlear implantation in a patient with congenital microtia, cochlear hypoplasia, venous anomalies of the temporal bone and laryngomalacia: Challenges and surgical considerationsXue Gao, Juan Zhao, Guan-Hua Li, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 22, 2008
SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing lossPu Dai, Qi Li, Deliang Huang, 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.
Zhonghua Yi Xue Za Zhi|August 4, 2007
[Genetic counseling and intervention for families with deaf-mute patients based on genetic testing: analysis of 5 families]Pu Dai, Bing Han, Yong-yi Yuan, et al.
Human Genetics|December 4, 2008
Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31Xue-Zhong Liu, Yongyi Yuan, Denise Yan, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|February 28, 2008
[Features of nationwide distribution and frequency of a common gap junction beta-2 gene mutation in China]Pu Dai, Fei Yu, Bing Han, et al.
BMC Medical Genomics|November 19, 2022
Addition of an affected family member to a previously ascertained autosomal recessive nonsyndromic hearing loss pedigree and systematic phenotype-genotype analysis of splice-site variants in MYO15AJin-Yuan Yang, Wei-Qian Wang, Ming-Yu Han, et al.
Pageof 22

Showing results (191-200 of 218) with videos related to

Sort By:
Pageof 22
Journal of Human Genetics|December 15, 2010
Novel missense mutations in MYO7A underlying postlingual high- or low-frequency non-syndromic hearing impairment in two large families from ChinaYi Sun, Jing Chen, Hanjun Sun, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|September 30, 2006
[Patients suffered from enlarged vestibular aqueduct syndrome in Chifeng deaf and dumb school detected by Pendred's syndrome gene hot spot mutation screening]Pu Dai, Xiu-Hui Zhu, Yong-Yi Yuan, 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.
Medicine|February 17, 2023
Cochlear implantation in a patient with congenital microtia, cochlear hypoplasia, venous anomalies of the temporal bone and laryngomalacia: Challenges and surgical considerationsXue Gao, Juan Zhao, Guan-Hua Li, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 22, 2008
SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing lossPu Dai, Qi Li, Deliang Huang, 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.
Zhonghua Yi Xue Za Zhi|August 4, 2007
[Genetic counseling and intervention for families with deaf-mute patients based on genetic testing: analysis of 5 families]Pu Dai, Bing Han, Yong-yi Yuan, et al.
Human Genetics|December 4, 2008
Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31Xue-Zhong Liu, Yongyi Yuan, Denise Yan, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|February 28, 2008
[Features of nationwide distribution and frequency of a common gap junction beta-2 gene mutation in China]Pu Dai, Fei Yu, Bing Han, et al.
BMC Medical Genomics|November 19, 2022
Addition of an affected family member to a previously ascertained autosomal recessive nonsyndromic hearing loss pedigree and systematic phenotype-genotype analysis of splice-site variants in MYO15AJin-Yuan Yang, Wei-Qian Wang, Ming-Yu Han, et al.
Pageof 22