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X M Ouyang

Showing results (1-10 of 8) with videos related to

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Journal of Medical Genetics|June 17, 2005
A novel locus for autosomal dominant non-syndromic deafness, DFNA53, maps to chromosome 14q11.2-q12D Yan, X Ke, S H Blanton, et al.
Clinical Genetics|March 18, 2004
Mutational spectrum in Usher syndrome type IIX M Ouyang, D Yan, J F Hejtmancik, 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.
Clinical Genetics|March 13, 2003
USH1C: a rare cause of USH1 in a non-Acadian population and a founder effect of the Acadian alleleX M Ouyang, J F Hejtmancik, S G Jacobson, et al.
Human Molecular Genetics|December 14, 2001
Mutations in GJA1 (connexin 43) are associated with non-syndromic autosomal recessive deafnessX Z Liu, X J Xia, J Adams, et al.
Zhonghua Bing Li Xue Za Zhi = Chinese Journal of Pathology|May 23, 2018
[Clinicopathologic and molecular features of cribriform morular variant of papillary thyroid carcinoma]X J Cui, H O Zhao, P Su, et al.
Journal of Molecular Biology|February 9, 2006
An isoform of GTPase regulator DOCK4 localizes to the stereocilia in the inner ear and binds to harmonin (USH1C)D Yan, F Li, M L Hall, et al.
Clinical Genetics|September 18, 2007
A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late-onset non-syndromic hearing loss in a Chinese familyJ Cheng, D Y Han, P Dai, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Journal of Medical Genetics|June 17, 2005
A novel locus for autosomal dominant non-syndromic deafness, DFNA53, maps to chromosome 14q11.2-q12D Yan, X Ke, S H Blanton, et al.
Clinical Genetics|March 18, 2004
Mutational spectrum in Usher syndrome type IIX M Ouyang, D Yan, J F Hejtmancik, 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.
Clinical Genetics|March 13, 2003
USH1C: a rare cause of USH1 in a non-Acadian population and a founder effect of the Acadian alleleX M Ouyang, J F Hejtmancik, S G Jacobson, et al.
Human Molecular Genetics|December 14, 2001
Mutations in GJA1 (connexin 43) are associated with non-syndromic autosomal recessive deafnessX Z Liu, X J Xia, J Adams, et al.
Zhonghua Bing Li Xue Za Zhi = Chinese Journal of Pathology|May 23, 2018
[Clinicopathologic and molecular features of cribriform morular variant of papillary thyroid carcinoma]X J Cui, H O Zhao, P Su, et al.
Journal of Molecular Biology|February 9, 2006
An isoform of GTPase regulator DOCK4 localizes to the stereocilia in the inner ear and binds to harmonin (USH1C)D Yan, F Li, M L Hall, et al.
Clinical Genetics|September 18, 2007
A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late-onset non-syndromic hearing loss in a Chinese familyJ Cheng, D Y Han, P Dai, et al.
Pageof 1