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

Lingji Chen

Showing results (31-40 of 36) with videos related to

Pageof 4
Sort By:
You have reached the last page of results.This site can display upto 36 results.
Laboratory Medicine|September 2, 2022
Application of the Single-Molecule Real-Time Technology (SMRT) for Identification of HKαα Thalassemia AlleleMin Zhang, Zhaodong Lin, Meihuan Chen, et al.
Frontiers in Pediatrics|May 2, 2025
Incidental finding of a <i>DMD</i> exons 48-55 deletion during prenatal diagnosisMin Zhang, Zhaodong Lin, Meihuan Chen, et al.
Journal of Human Genetics|July 27, 2022
Prenatal diagnosis of fetuses with region of homozygosity detected by single nucleotide polymorphism array: a retrospective cohort studyBin Liang, Donghong Yu, Wantong Zhao, et al.
BMC Musculoskeletal Disorders|January 15, 2025
Congenital muscular dystrophies and myopathies: the leading cause of genetic muscular disorders in eleven Chinese familiesBin Mao, Xiaoling Cai, Na Lin, et al.
Clinical Genetics|December 20, 2022
A novel PLS1 c.981+1G>A variant causes autosomal-dominant hereditary hearing loss in a familyLiangpu Xu, Xinrui Wang, Jia Li, et al.
The Journal of Molecular Diagnostics : JMD|June 1, 2020
Long-Molecule Sequencing: A New Approach for Identification of Clinically Significant DNA Variants in α-Thalassemia and β-Thalassemia CarriersLiangpu Xu, Aiping Mao, Hui Liu, et al.
Pageof 4

Showing results (31-40 of 36) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 36 results.
Laboratory Medicine|September 2, 2022
Application of the Single-Molecule Real-Time Technology (SMRT) for Identification of HKαα Thalassemia AlleleMin Zhang, Zhaodong Lin, Meihuan Chen, et al.
Frontiers in Pediatrics|May 2, 2025
Incidental finding of a <i>DMD</i> exons 48-55 deletion during prenatal diagnosisMin Zhang, Zhaodong Lin, Meihuan Chen, et al.
Journal of Human Genetics|July 27, 2022
Prenatal diagnosis of fetuses with region of homozygosity detected by single nucleotide polymorphism array: a retrospective cohort studyBin Liang, Donghong Yu, Wantong Zhao, et al.
BMC Musculoskeletal Disorders|January 15, 2025
Congenital muscular dystrophies and myopathies: the leading cause of genetic muscular disorders in eleven Chinese familiesBin Mao, Xiaoling Cai, Na Lin, et al.
Clinical Genetics|December 20, 2022
A novel PLS1 c.981+1G>A variant causes autosomal-dominant hereditary hearing loss in a familyLiangpu Xu, Xinrui Wang, Jia Li, et al.
The Journal of Molecular Diagnostics : JMD|June 1, 2020
Long-Molecule Sequencing: A New Approach for Identification of Clinically Significant DNA Variants in α-Thalassemia and β-Thalassemia CarriersLiangpu Xu, Aiping Mao, Hui Liu, et al.
Pageof 4