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David G Hunter

Showing results (161-170 of 185) with videos related to

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JAMA Ophthalmology|September 5, 2024
Race, Ethnicity, and Sex in Pediatric Eye Disease Investigator Group Clinical StudiesQais A Dihan, Ahmad F Alzein, Othman M Ibrahim, et al.
American Journal of Medical Genetics. Part A|December 8, 2015
Two unique TUBB3 mutations cause both CFEOM3 and malformations of cortical developmentMary C Whitman, Caroline Andrews, Wai-Man Chan, et al.
American Journal of Human Genetics|May 17, 2016
Loss of MAFB Function in Humans and Mice Causes Duane Syndrome, Aberrant Extraocular Muscle Innervation, and Inner-Ear DefectsJong G Park, Max A Tischfield, Alicia A Nugent, et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|June 10, 2020
In Vivo Quasi-Elastic Light Scattering Eye Scanner Detects Molecular Aging in HumansOlga Minaeva, Srikant Sarangi, Danielle M Ledoux, et al.
American Journal of Ophthalmology|June 24, 2022
Nasal Transposition of the Split Lateral Rectus Muscle for Strabismus Associated With Bilateral 3<sup>rd</sup>-Nerve PalsyIsdin Oke, Birgit Lorenz, Sotirios Basiakos, et al.
Brain : a Journal of Neurology|February 10, 2011
The clinical and molecular genetic features of idiopathic infantile periodic alternating nystagmusMervyn G Thomas, Moira Crosier, Susan Lindsay, et al.
American Journal of Human Genetics|July 10, 2012
HOXB1 founder mutation in humans recapitulates the phenotype of Hoxb1-/- miceBryn D Webb, Sherin Shaaban, Harald Gaspar, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|November 13, 2022
Extraocular muscle ductions following nasal transposition of the split lateral rectus muscleIsdin Oke, Birgit Lorenz, Sotirios Basiakos, et al.
Plos One|May 27, 2010
Alzheimer's disease amyloid-beta links lens and brain pathology in Down syndromeJuliet A Moncaster, Roberto Pineda, Robert D Moir, et al.
BMC Genetics|May 22, 2007
Three novel mutations in KIF21A highlight the importance of the third coiled-coil stalk domain in the etiology of CFEOM1Wai-Man Chan, Caroline Andrews, Laryssa Dragan, et al.
Pageof 19

Showing results (161-170 of 185) with videos related to

Sort By:
Pageof 19
JAMA Ophthalmology|September 5, 2024
Race, Ethnicity, and Sex in Pediatric Eye Disease Investigator Group Clinical StudiesQais A Dihan, Ahmad F Alzein, Othman M Ibrahim, et al.
American Journal of Medical Genetics. Part A|December 8, 2015
Two unique TUBB3 mutations cause both CFEOM3 and malformations of cortical developmentMary C Whitman, Caroline Andrews, Wai-Man Chan, et al.
American Journal of Human Genetics|May 17, 2016
Loss of MAFB Function in Humans and Mice Causes Duane Syndrome, Aberrant Extraocular Muscle Innervation, and Inner-Ear DefectsJong G Park, Max A Tischfield, Alicia A Nugent, et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|June 10, 2020
In Vivo Quasi-Elastic Light Scattering Eye Scanner Detects Molecular Aging in HumansOlga Minaeva, Srikant Sarangi, Danielle M Ledoux, et al.
American Journal of Ophthalmology|June 24, 2022
Nasal Transposition of the Split Lateral Rectus Muscle for Strabismus Associated With Bilateral 3<sup>rd</sup>-Nerve PalsyIsdin Oke, Birgit Lorenz, Sotirios Basiakos, et al.
Brain : a Journal of Neurology|February 10, 2011
The clinical and molecular genetic features of idiopathic infantile periodic alternating nystagmusMervyn G Thomas, Moira Crosier, Susan Lindsay, et al.
American Journal of Human Genetics|July 10, 2012
HOXB1 founder mutation in humans recapitulates the phenotype of Hoxb1-/- miceBryn D Webb, Sherin Shaaban, Harald Gaspar, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|November 13, 2022
Extraocular muscle ductions following nasal transposition of the split lateral rectus muscleIsdin Oke, Birgit Lorenz, Sotirios Basiakos, et al.
Plos One|May 27, 2010
Alzheimer's disease amyloid-beta links lens and brain pathology in Down syndromeJuliet A Moncaster, Roberto Pineda, Robert D Moir, et al.
BMC Genetics|May 22, 2007
Three novel mutations in KIF21A highlight the importance of the third coiled-coil stalk domain in the etiology of CFEOM1Wai-Man Chan, Caroline Andrews, Laryssa Dragan, et al.
Pageof 19