Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

X Z Liu

Showing results (181-190 of 191) with videos related to

Pageof 20
Sort By:
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 deafnessH-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 familiesH 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 familyJ 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 geneM 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 publicationA 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 CDH23J 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.
Pageof 20

Showing results (181-190 of 191) with videos related to

Sort By:
Pageof 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 deafnessH-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 familiesH 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 familyJ 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 geneM 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 publicationA 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 CDH23J 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.
Pageof 20