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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.
Zhonghua Jie He He Hu Xi Za Zhi = Zhonghua Jiehe He Huxi Zazhi = Chinese Journal of Tuberculosis and Respiratory Diseases
|
July 14, 2021
[Preliminary clinical observation of omalizumab therapy for moderate to severe asthma]
P H Wu, C Dong, J X Xie, et al.
Genetics and Molecular Research : GMR
|
October 6, 2016
Cinnamon effectively inhibits the activity of leukemia stem cells
X Guan, M C Su, R B Zhao, 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.
Developments in Biologicals
|
September 27, 2008
Using integrative genomics to elucidate genetic resistance to Marek's disease in chickens
H Cheng, M Niikura, T Kim, et al.
Zhonghua Nei Ke Za Zhi
|
January 25, 2025
[The characteristics and associated factors of hand dysfunction in patients with rheumatoid arthritis]
Y W Zou, Y Yang, Z M Ouyang, 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 family
J Cheng, D Y Han, P Dai, et al.
Nature
|
April 7, 2022
Brain charts for the human lifespan
R A I Bethlehem, J Seidlitz, S R White, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 50) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 50 results.
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.
Zhonghua Jie He He Hu Xi Za Zhi = Zhonghua Jiehe He Huxi Zazhi = Chinese Journal of Tuberculosis and Respiratory Diseases
|
July 14, 2021
[Preliminary clinical observation of omalizumab therapy for moderate to severe asthma]
P H Wu, C Dong, J X Xie, et al.
Genetics and Molecular Research : GMR
|
October 6, 2016
Cinnamon effectively inhibits the activity of leukemia stem cells
X Guan, M C Su, R B Zhao, 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.
Developments in Biologicals
|
September 27, 2008
Using integrative genomics to elucidate genetic resistance to Marek's disease in chickens
H Cheng, M Niikura, T Kim, et al.
Zhonghua Nei Ke Za Zhi
|
January 25, 2025
[The characteristics and associated factors of hand dysfunction in patients with rheumatoid arthritis]
Y W Zou, Y Yang, Z M Ouyang, 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 family
J Cheng, D Y Han, P Dai, et al.
Nature
|
April 7, 2022
Brain charts for the human lifespan
R A I Bethlehem, J Seidlitz, S R White, et al.
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of 5