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

Qianjun Zhang

Showing results (41-50 of 74) with videos related to

Pageof 8
Sort By:
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|March 27, 2023
[Genetic analysis and reproductive intervention of 7 families with gonadal mosaicism for Duchenne muscular dystrophy]Bodi Gao, Xiaowen Yang, Xiao Hu, et al.
Hereditas|October 4, 2018
Long-read sequencing identified a causal structural variant in an exome-negative case and enabled preimplantation genetic diagnosisHefan Miao, Jiapeng Zhou, Qi Yang, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 16, 2021
RNF216 regulates meiosis and PKA stability in the testesDengfeng Li, Fangfang Li, Lanlan Meng, et al.
Journal of Assisted Reproduction and Genetics|December 10, 2025
Novel INSL3 variants cause male infertility with cryptorchidismChunjia Wei, Wenqing Lu, Yong Li, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|September 9, 2022
[Genetic testing and prenatal diagnosis of 671 Chinese pedigrees affected with Duchenne/Becker muscular dystrophy]Shikun Luo, Wenbin He, Xiaomeng Zhao, et al.
Scientific Reports|November 7, 2014
Hot pressing to enhance the transport Jc of Sr0.6K0.4Fe2As2 superconducting tapesHe Lin, Chao Yao, Xianping Zhang, et al.
Genes|November 11, 2022
Reclassification of <i>DMD</i> Duplications as Benign: Recommendations for Cautious Interpretation of Variants Identified in Prenatal ScreeningWenbin He, Guiquan Meng, Xiao Hu, et al.
Journal of Assisted Reproduction and Genetics|March 16, 2024
Identification of novel homozygous asthenoteratospermia-causing ARMC2 mutations associated with multiple morphological abnormalities of the sperm flagellaSiyi Zhao, Qiong Liu, Lilan Su, et al.
Journal of Assisted Reproduction and Genetics|April 3, 2024
Novel SPEF2 variants cause male infertility and likely primary ciliary dyskinesiaWenqing Lu, Yong Li, Lanlan Meng, et al.
Clinical Genetics|December 17, 2022
Novel homozygous variant of CCIN causes male infertility owing to the abnormal sperm head with a nuclear subsidence phenotypeJiaxin He, Qiang Liu, Weili Wang, et al.
Pageof 8

Showing results (41-50 of 74) with videos related to

Sort By:
Pageof 8
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|March 27, 2023
[Genetic analysis and reproductive intervention of 7 families with gonadal mosaicism for Duchenne muscular dystrophy]Bodi Gao, Xiaowen Yang, Xiao Hu, et al.
Hereditas|October 4, 2018
Long-read sequencing identified a causal structural variant in an exome-negative case and enabled preimplantation genetic diagnosisHefan Miao, Jiapeng Zhou, Qi Yang, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 16, 2021
RNF216 regulates meiosis and PKA stability in the testesDengfeng Li, Fangfang Li, Lanlan Meng, et al.
Journal of Assisted Reproduction and Genetics|December 10, 2025
Novel INSL3 variants cause male infertility with cryptorchidismChunjia Wei, Wenqing Lu, Yong Li, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|September 9, 2022
[Genetic testing and prenatal diagnosis of 671 Chinese pedigrees affected with Duchenne/Becker muscular dystrophy]Shikun Luo, Wenbin He, Xiaomeng Zhao, et al.
Scientific Reports|November 7, 2014
Hot pressing to enhance the transport Jc of Sr0.6K0.4Fe2As2 superconducting tapesHe Lin, Chao Yao, Xianping Zhang, et al.
Genes|November 11, 2022
Reclassification of <i>DMD</i> Duplications as Benign: Recommendations for Cautious Interpretation of Variants Identified in Prenatal ScreeningWenbin He, Guiquan Meng, Xiao Hu, et al.
Journal of Assisted Reproduction and Genetics|March 16, 2024
Identification of novel homozygous asthenoteratospermia-causing ARMC2 mutations associated with multiple morphological abnormalities of the sperm flagellaSiyi Zhao, Qiong Liu, Lilan Su, et al.
Journal of Assisted Reproduction and Genetics|April 3, 2024
Novel SPEF2 variants cause male infertility and likely primary ciliary dyskinesiaWenqing Lu, Yong Li, Lanlan Meng, et al.
Clinical Genetics|December 17, 2022
Novel homozygous variant of CCIN causes male infertility owing to the abnormal sperm head with a nuclear subsidence phenotypeJiaxin He, Qiang Liu, Weili Wang, et al.
Pageof 8