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Zhonghua Wei Chang Wai Ke Za Zhi = Chinese Journal of Gastrointestinal Surgery
|
June 27, 2019
["Watch and wait" strategy after neoadjuvant therapy for rectal cancer: status survey of perceptions, attitudes and treatment selection in Chinese surgeons]
T T Sun, L Wang, Y F Yao, et al.
Zhonghua Wai Ke Za Zhi [Chinese Journal of Surgery]
|
April 29, 2026
[Three-year survival outcomes of neoadjuvant immunotherapy for local advanced rectal cancer with pMMR: a single-center report of 140 patients from Peking University Cancer Hospital]
M H Zhao, B Y Qu, Y L Huang, et al.
Zhonghua Yu Fang Yi Xue Za Zhi [Chinese Journal of Preventive Medicine]
|
November 13, 2022
[Application of pretrained model based on electronic medical record in recognition of acute respiratory infection]
M M Jia, X Z Liu, L Qi, et al.
Journal of Medical Genetics
|
April 5, 2003
Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness
H-J Park, S Shaukat, X-Z Liu, et al.
Clinical Genetics
|
March 4, 2008
Novel mutations in the vWFA2 domain of COCH in two Chinese DFNA9 families
H J Yuan, D Y Han, Q Sun, 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 Genetics
|
September 6, 2000
A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene
M Bitner-Glindzicz, K J Lindley, P Rutland, et al.
Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi
|
November 7, 2025
Molecular stratification of gliomas using next-generation sequencing: abridged secondary publication
A K Y Chan, D T M Chan, J Y T Chan, et al.
American Journal of Human Genetics
|
November 25, 2000
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23
J M Bork, L M Peters, S Riazuddin, et al.
Zhonghua Bing Li Xue Za Zhi = Chinese Journal of Pathology
|
March 16, 2020
[A pathological report of three COVID-19 cases by minimal invasive autopsies]
X H Yao, T Y Li, Z C He, et al.
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Search research articles
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Showing results (181-190 of 191) with videos related to
Sort By:
Page
of 20
Zhonghua Wei Chang Wai Ke Za Zhi = Chinese Journal of Gastrointestinal Surgery
|
June 27, 2019
["Watch and wait" strategy after neoadjuvant therapy for rectal cancer: status survey of perceptions, attitudes and treatment selection in Chinese surgeons]
T T Sun, L Wang, Y F Yao, et al.
Zhonghua Wai Ke Za Zhi [Chinese Journal of Surgery]
|
April 29, 2026
[Three-year survival outcomes of neoadjuvant immunotherapy for local advanced rectal cancer with pMMR: a single-center report of 140 patients from Peking University Cancer Hospital]
M H Zhao, B Y Qu, Y L Huang, et al.
Zhonghua Yu Fang Yi Xue Za Zhi [Chinese Journal of Preventive Medicine]
|
November 13, 2022
[Application of pretrained model based on electronic medical record in recognition of acute respiratory infection]
M M Jia, X Z Liu, L Qi, et al.
Journal of Medical Genetics
|
April 5, 2003
Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness
H-J Park, S Shaukat, X-Z Liu, et al.
Clinical Genetics
|
March 4, 2008
Novel mutations in the vWFA2 domain of COCH in two Chinese DFNA9 families
H J Yuan, D Y Han, Q Sun, 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 Genetics
|
September 6, 2000
A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene
M Bitner-Glindzicz, K J Lindley, P Rutland, et al.
Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi
|
November 7, 2025
Molecular stratification of gliomas using next-generation sequencing: abridged secondary publication
A K Y Chan, D T M Chan, J Y T Chan, et al.
American Journal of Human Genetics
|
November 25, 2000
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23
J M Bork, L M Peters, S Riazuddin, et al.
Zhonghua Bing Li Xue Za Zhi = Chinese Journal of Pathology
|
March 16, 2020
[A pathological report of three COVID-19 cases by minimal invasive autopsies]
X H Yao, T Y Li, Z C He, et al.
Page
of 20