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Clinical Genetics
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November 15, 2005
Assessment of the genetic causes of recessive childhood non-syndromic deafness in the UK - implications for genetic testing
T Hutchin, N N Coy, H Conlon, 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 allele
X M Ouyang, J F Hejtmancik, S G Jacobson, et al.
Zhongguo Ji Sheng Chong Xue Yu Ji Sheng Chong Bing Za Zhi = Chinese Journal of Parasitology & Parasitic Diseases
|
January 1, 1991
[Eighty cases of alveolar hydatid disease treated with albendazole]
M Li, W X Li, X Z Liu, et al.
European Review for Medical and Pharmacological Sciences
|
December 4, 2020
The dual role of anti-viral therapy in the treatment of Coronavirus disease 2019
J-Y Liu, M-X Hua, C-J Du, et al.
European Review for Medical and Pharmacological Sciences
|
March 23, 2021
Author Correction: The dual role of anti-viral therapy in the treatment of Coronavirus disease 2019
J-Y Liu, M-X Hua, C-J Du, et al.
Clinical Genetics
|
September 5, 2001
Haplotype analysis of the USH1D locus and genotype-phenotype correlations
X Z Liu, S H Blanton, M Bitner-Glindzicz, et al.
Human Molecular Genetics
|
December 14, 2001
Mutations in GJA1 (connexin 43) are associated with non-syndromic autosomal recessive deafness
X Z Liu, X J Xia, J Adams, et al.
American Journal of Human Genetics
|
August 27, 1998
Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndrome
X Z Liu, C Hope, J Walsh, et al.
Zhonghua Yi Xue Za Zhi
|
December 26, 2017
[Efficacy and safety of transbronchial cryobiopsy in the etiologic diagnosis of diffuse lung disease]
Y S Li, S L Guo, X H Yi, 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.
Page
of 20
Search research articles
Search
Showing results (161-170 of 191) with videos related to
Sort By:
Page
of 20
Clinical Genetics
|
November 15, 2005
Assessment of the genetic causes of recessive childhood non-syndromic deafness in the UK - implications for genetic testing
T Hutchin, N N Coy, H Conlon, 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 allele
X M Ouyang, J F Hejtmancik, S G Jacobson, et al.
Zhongguo Ji Sheng Chong Xue Yu Ji Sheng Chong Bing Za Zhi = Chinese Journal of Parasitology & Parasitic Diseases
|
January 1, 1991
[Eighty cases of alveolar hydatid disease treated with albendazole]
M Li, W X Li, X Z Liu, et al.
European Review for Medical and Pharmacological Sciences
|
December 4, 2020
The dual role of anti-viral therapy in the treatment of Coronavirus disease 2019
J-Y Liu, M-X Hua, C-J Du, et al.
European Review for Medical and Pharmacological Sciences
|
March 23, 2021
Author Correction: The dual role of anti-viral therapy in the treatment of Coronavirus disease 2019
J-Y Liu, M-X Hua, C-J Du, et al.
Clinical Genetics
|
September 5, 2001
Haplotype analysis of the USH1D locus and genotype-phenotype correlations
X Z Liu, S H Blanton, M Bitner-Glindzicz, et al.
Human Molecular Genetics
|
December 14, 2001
Mutations in GJA1 (connexin 43) are associated with non-syndromic autosomal recessive deafness
X Z Liu, X J Xia, J Adams, et al.
American Journal of Human Genetics
|
August 27, 1998
Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndrome
X Z Liu, C Hope, J Walsh, et al.
Zhonghua Yi Xue Za Zhi
|
December 26, 2017
[Efficacy and safety of transbronchial cryobiopsy in the etiologic diagnosis of diffuse lung disease]
Y S Li, S L Guo, X H Yi, 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.
Page
of 20