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

Ophthalmic genetics

Showing results (41-50 of 2,050) with videos related to

Pageof 205
Sort By:
Ophthalmic Genetics|September 23, 2025
<i>ADAMTSL4</i> ectopia lentis associated with Poland syndrome: a case reportDaniel Cool, Shuan Dai, Allister Lee
Ophthalmic Genetics|January 15, 2020
A founder <i>RDH5</i> splice site mutation leads to retinitis punctata albescens in two inbred Pakistani kindredsRizwan Khan, Rana Muhammad Kamran Shabbir, Irum Raza, et al.
Ophthalmic Genetics|August 29, 2020
Assessment of incorporation of the International Committee for Classification of Corneal Dystrophies (IC3D) in literatureSaif Aldeen AlRyalat, Bahaa Al-Din Jaber
Ophthalmic Genetics|March 12, 2020
Corneal endothelial cell abnormalities in X-linked Alport syndromeEleanor Nicklason, Heather Mack, Jacqueline Beltz, et al.
Ophthalmic Genetics|March 24, 2020
Illustration of tessellation in Down syndromeLavinia Postolache, Casper De Jong, Georges Casimir
Ophthalmic Genetics|March 17, 2020
Quasidominance in autosomal recessive <i>RDH12</i>-Leber congenital amaurosisRuben Jauregui, Ahra Cho, Christine L Xu, et al.
Ophthalmic Genetics|October 28, 2020
<i>SIX6</i>-related anophthalmia/microphthalmia: second report on a deletion in a consanguineous familyAsha Deepthi, Omar Fakhoury, Mohamad Daher, et al.
Ophthalmic Genetics|July 9, 2021
Clinical and molecular findings in patients with pattern dystrophyAndrea Sodi, Dario Pasquale Mucciolo, Dario Giorgio, et al.
Ophthalmic Genetics|July 20, 2021
Identification of a novel nonsense variant in <i>FYCO1</i> gene associated with infantile cataract and cortical atrophyRaffi Aprahamian, T Yammine, N Salem, et al.
Ophthalmic Genetics|July 24, 2024
Genetic methylation in myopiaXi He, Shi-Ming Li
Pageof 205

Showing results (41-50 of 2,050) with videos related to

Sort By:
Pageof 205
Ophthalmic Genetics|September 23, 2025
<i>ADAMTSL4</i> ectopia lentis associated with Poland syndrome: a case reportDaniel Cool, Shuan Dai, Allister Lee
Ophthalmic Genetics|January 15, 2020
A founder <i>RDH5</i> splice site mutation leads to retinitis punctata albescens in two inbred Pakistani kindredsRizwan Khan, Rana Muhammad Kamran Shabbir, Irum Raza, et al.
Ophthalmic Genetics|August 29, 2020
Assessment of incorporation of the International Committee for Classification of Corneal Dystrophies (IC3D) in literatureSaif Aldeen AlRyalat, Bahaa Al-Din Jaber
Ophthalmic Genetics|March 12, 2020
Corneal endothelial cell abnormalities in X-linked Alport syndromeEleanor Nicklason, Heather Mack, Jacqueline Beltz, et al.
Ophthalmic Genetics|March 24, 2020
Illustration of tessellation in Down syndromeLavinia Postolache, Casper De Jong, Georges Casimir
Ophthalmic Genetics|March 17, 2020
Quasidominance in autosomal recessive <i>RDH12</i>-Leber congenital amaurosisRuben Jauregui, Ahra Cho, Christine L Xu, et al.
Ophthalmic Genetics|October 28, 2020
<i>SIX6</i>-related anophthalmia/microphthalmia: second report on a deletion in a consanguineous familyAsha Deepthi, Omar Fakhoury, Mohamad Daher, et al.
Ophthalmic Genetics|July 9, 2021
Clinical and molecular findings in patients with pattern dystrophyAndrea Sodi, Dario Pasquale Mucciolo, Dario Giorgio, et al.
Ophthalmic Genetics|July 20, 2021
Identification of a novel nonsense variant in <i>FYCO1</i> gene associated with infantile cataract and cortical atrophyRaffi Aprahamian, T Yammine, N Salem, et al.
Ophthalmic Genetics|July 24, 2024
Genetic methylation in myopiaXi He, Shi-Ming Li
Pageof 205