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Morag E Shanks

Showing results (1-10 of 16) with videos related to

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Ocular Immunology and Inflammation|October 18, 2017
Two Novel CAPN5 Variants Associated with Mild and Severe Autosomal Dominant Neovascular Inflammatory Vitreoretinopathy PhenotypesNadia M Randazzo, Morag E Shanks, Penny Clouston, et al.
Ophthalmic Genetics|December 2, 2017
A splice-site variant in FLVCR1 produces retinitis pigmentosa without posterior column ataxiaImran H Yusuf, Morag E Shanks, Penny Clouston, et al.
American Journal of Ophthalmology|February 8, 2019
The Location of Exon 4 Mutations in RP1 Raises Challenges for Genetic Counseling and Gene TherapyAnika Nanda, Michelle E McClements, Penny Clouston, et al.
American Journal of Physical Anthropology|February 3, 2007
Thomas Jefferson's Y chromosome belongs to a rare European lineageTuri E King, Georgina R Bowden, Patricia L Balaresque, et al.
JAMA Ophthalmology|September 6, 2019
Clinical Characterization of Retinitis Pigmentosa Associated With Variants in SNRNP200Imran H Yusuf, Johannes Birtel, Morag E Shanks, et al.
Eye (London, England)|July 31, 2020
"Genetic and clinical findings in an ethnically diverse retinitis pigmentosa cohort associated with pathogenic variants in EYS"Olivia Cundy, Suzanne Broadgate, Stephanie Halford, et al.
Mutation Research|May 12, 2009
The effects of in utero irradiation on mutation induction and transgenerational instability in miceRuth C Barber, Robert J Hardwick, Morag E Shanks, et al.
Mutation Research|October 22, 2008
Complex germline and somatic mutation processes at a haploid human minisatellite shown by single-molecule analysisMorag E Shanks, Celia A May, Yuri E Dubrova, et al.
BMC Ophthalmology|April 10, 2021
Targeted next generation sequencing and family survey enable correct genetic diagnosis in CRX associated macular dystrophy - a case reportSaoud Al-Khuzaei, Karl A Z Hudspith, Suzanne Broadgate, et al.
JAMA Network Open|June 15, 2019
Clinical and Molecular Characterization of PROM1-Related Retinal DegenerationJasmina Cehajic-Kapetanovic, Johannes Birtel, Michelle E McClements, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Ocular Immunology and Inflammation|October 18, 2017
Two Novel CAPN5 Variants Associated with Mild and Severe Autosomal Dominant Neovascular Inflammatory Vitreoretinopathy PhenotypesNadia M Randazzo, Morag E Shanks, Penny Clouston, et al.
Ophthalmic Genetics|December 2, 2017
A splice-site variant in FLVCR1 produces retinitis pigmentosa without posterior column ataxiaImran H Yusuf, Morag E Shanks, Penny Clouston, et al.
American Journal of Ophthalmology|February 8, 2019
The Location of Exon 4 Mutations in RP1 Raises Challenges for Genetic Counseling and Gene TherapyAnika Nanda, Michelle E McClements, Penny Clouston, et al.
American Journal of Physical Anthropology|February 3, 2007
Thomas Jefferson's Y chromosome belongs to a rare European lineageTuri E King, Georgina R Bowden, Patricia L Balaresque, et al.
JAMA Ophthalmology|September 6, 2019
Clinical Characterization of Retinitis Pigmentosa Associated With Variants in SNRNP200Imran H Yusuf, Johannes Birtel, Morag E Shanks, et al.
Eye (London, England)|July 31, 2020
"Genetic and clinical findings in an ethnically diverse retinitis pigmentosa cohort associated with pathogenic variants in EYS"Olivia Cundy, Suzanne Broadgate, Stephanie Halford, et al.
Mutation Research|May 12, 2009
The effects of in utero irradiation on mutation induction and transgenerational instability in miceRuth C Barber, Robert J Hardwick, Morag E Shanks, et al.
Mutation Research|October 22, 2008
Complex germline and somatic mutation processes at a haploid human minisatellite shown by single-molecule analysisMorag E Shanks, Celia A May, Yuri E Dubrova, et al.
BMC Ophthalmology|April 10, 2021
Targeted next generation sequencing and family survey enable correct genetic diagnosis in CRX associated macular dystrophy - a case reportSaoud Al-Khuzaei, Karl A Z Hudspith, Suzanne Broadgate, et al.
JAMA Network Open|June 15, 2019
Clinical and Molecular Characterization of PROM1-Related Retinal DegenerationJasmina Cehajic-Kapetanovic, Johannes Birtel, Michelle E McClements, et al.
Pageof 2