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

Molly Marra

Showing results (11-20 of 15) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 15 results.
Biorxiv : the Preprint Server for Biology|February 15, 2023
Systematic assessment of the contribution of structural variants to inherited retinal diseasesShu Wen, Meng Wang, Xinye Qian, et al.
Human Molecular Genetics|February 22, 2023
Systematic assessment of the contribution of structural variants to inherited retinal diseasesShu Wen, Meng Wang, Xinye Qian, et al.
Human Molecular Genetics|March 7, 2024
Comparative analysis of in-silico tools in identifying pathogenic variants in dominant inherited retinal diseasesDaniel C Brock, Meng Wang, Hafiz Muhammad Jafar Hussain, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 29, 2024
Loss-of-function variants in UBAP1L cause autosomal recessive retinal degenerationJi Hoon Han, Kim Rodenburg, Tamar Hayman, et al.
NPJ Genomic Medicine|April 17, 2025
Variants in CFAP410 cause a range of retinal and skeletal phenotypesRyan E Schmidt, Amy E Pohodich, David Birch, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Biorxiv : the Preprint Server for Biology|February 15, 2023
Systematic assessment of the contribution of structural variants to inherited retinal diseasesShu Wen, Meng Wang, Xinye Qian, et al.
Human Molecular Genetics|February 22, 2023
Systematic assessment of the contribution of structural variants to inherited retinal diseasesShu Wen, Meng Wang, Xinye Qian, et al.
Human Molecular Genetics|March 7, 2024
Comparative analysis of in-silico tools in identifying pathogenic variants in dominant inherited retinal diseasesDaniel C Brock, Meng Wang, Hafiz Muhammad Jafar Hussain, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 29, 2024
Loss-of-function variants in UBAP1L cause autosomal recessive retinal degenerationJi Hoon Han, Kim Rodenburg, Tamar Hayman, et al.
NPJ Genomic Medicine|April 17, 2025
Variants in CFAP410 cause a range of retinal and skeletal phenotypesRyan E Schmidt, Amy E Pohodich, David Birch, et al.
Pageof 2