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X M Ke

Showing results (1-10 of 7) with videos related to

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Zhonghua Er Bi Yan Hou Ke Za Zhi|January 1, 1993
[Analysis of evoked otoacoustic emissions in patients with high frequency cochlear hearing loss]X M Ke
Lin Chuang Er Bi Yan Hou Ke Za Zhi = Journal of Clinical Otorhinolaryngology|January 25, 2003
[Nonsyndromic deafness and mitochondrial DNA mutation]Y H Liu, X M Ke, Z P Gu
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|September 28, 2017
Absorption mechanism of three curcumin constituents through in situ intestinal perfusion methodY-H Wang, X-M Ke, C-H Zhang, et al.
Lin Chuang Er Bi Yan Hou Ke Za Zhi = Journal of Clinical Otorhinolaryngology|January 25, 2003
[Measuring and analyzing of otoacoustic emission tests of a family with genetic progressive sensorineural hearing loss]H Yu, X M Ke, D L Yu, et al.
Lin Chuang Er Bi Yan Hou Ke Za Zhi = Journal of Clinical Otorhinolaryngology|January 25, 2003
[Genetic epidemiologic study of mitochondrial DNA 7445A-->G mutation among non-syndromic deafness in Chinese population]Y H Liu, X M Ke, Y Qi, et al.
Acta Oto-Laryngologica|June 24, 2008
Audiological and genetic features of the mtDNA mutationsX Z Liu, S Angeli, X M Ouyang, et al.
American Journal of Human Genetics|August 27, 1998
Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndromeX Z Liu, C Hope, J Walsh, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Zhonghua Er Bi Yan Hou Ke Za Zhi|January 1, 1993
[Analysis of evoked otoacoustic emissions in patients with high frequency cochlear hearing loss]X M Ke
Lin Chuang Er Bi Yan Hou Ke Za Zhi = Journal of Clinical Otorhinolaryngology|January 25, 2003
[Nonsyndromic deafness and mitochondrial DNA mutation]Y H Liu, X M Ke, Z P Gu
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|September 28, 2017
Absorption mechanism of three curcumin constituents through in situ intestinal perfusion methodY-H Wang, X-M Ke, C-H Zhang, et al.
Lin Chuang Er Bi Yan Hou Ke Za Zhi = Journal of Clinical Otorhinolaryngology|January 25, 2003
[Measuring and analyzing of otoacoustic emission tests of a family with genetic progressive sensorineural hearing loss]H Yu, X M Ke, D L Yu, et al.
Lin Chuang Er Bi Yan Hou Ke Za Zhi = Journal of Clinical Otorhinolaryngology|January 25, 2003
[Genetic epidemiologic study of mitochondrial DNA 7445A-->G mutation among non-syndromic deafness in Chinese population]Y H Liu, X M Ke, Y Qi, et al.
Acta Oto-Laryngologica|June 24, 2008
Audiological and genetic features of the mtDNA mutationsX Z Liu, S Angeli, X M Ouyang, et al.
American Journal of Human Genetics|August 27, 1998
Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndromeX Z Liu, C Hope, J Walsh, et al.
Pageof 1