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Jamie E Craig

Showing results (221-230 of 352) with videos related to

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Archives of Ophthalmology (Chicago, Ill. : 1960)|August 13, 2003
Glaucoma phenotype in pedigrees with the myocilin Thr377Met mutationDavid A Mackey, Danielle L Healey, John H Fingert, et al.
Hypertension (Dallas, Tex. : 1979)|August 19, 2009
Quantitative genetic analysis of the retinal vascular caliber: the Australian Twins Eye StudyCong Sun, Gu Zhu, Tien Y Wong, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|December 10, 2003
Hereditary hyperferritinemia-cataract syndrome: prevalence, lens morphology, spectrum of mutations, and clinical presentationsJamie E Craig, J Benedict Clark, Janet L McLeod, et al.
Investigative Ophthalmology & Visual Science|June 30, 2004
Spectrum and frequency of FZD4 mutations in familial exudative vitreoretinopathyCarmel Toomes, Helen M Bottomley, Sheila Scott, et al.
European Journal of Human Genetics : EJHG|March 27, 2026
Non-coding structural variants disrupting conserved PITX2 enhancer loci in Axenfeld-Rieger syndromeLucas A Mitchell, Joshua Schmidt, Emmanuelle Souzeau, et al.
Ophthalmology|March 5, 2013
Higher prevalence of myocilin mutations in advanced glaucoma in comparison with less advanced disease in an Australasian disease registryEmmanuelle Souzeau, Kathryn P Burdon, Andrew Dubowsky, et al.
Plos One|October 11, 2012
The p53 codon 72 PRO/PRO genotype may be associated with initial central visual field defects in caucasians with primary open angle glaucomaJaney L Wiggs, Alex W Hewitt, Bao Jian Fan, et al.
Medrxiv : the Preprint Server for Health Sciences|June 12, 2025
Axenfeld-Rieger syndrome associated with a megabase-scale inversion separating <i>PITX2</i> from a conserved enhancer locusLucas A Mitchell, Joshua Schmidt, Emmanuelle Souzeau, et al.
Ophthalmology|October 30, 2007
Genetic dissection of myopia: evidence for linkage of ocular axial length to chromosome 5qGu Zhu, Alex W Hewitt, Jonathan B Ruddle, et al.
Human Mutation|May 11, 2021
A novel GSN variant outside the G2 calcium-binding domain associated with Amyloidosis of the Finnish typeSean Mullany, Emmanuelle Souzeau, Sonja Klebe, et al.
Pageof 36

Showing results (221-230 of 352) with videos related to

Sort By:
Pageof 36
Archives of Ophthalmology (Chicago, Ill. : 1960)|August 13, 2003
Glaucoma phenotype in pedigrees with the myocilin Thr377Met mutationDavid A Mackey, Danielle L Healey, John H Fingert, et al.
Hypertension (Dallas, Tex. : 1979)|August 19, 2009
Quantitative genetic analysis of the retinal vascular caliber: the Australian Twins Eye StudyCong Sun, Gu Zhu, Tien Y Wong, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|December 10, 2003
Hereditary hyperferritinemia-cataract syndrome: prevalence, lens morphology, spectrum of mutations, and clinical presentationsJamie E Craig, J Benedict Clark, Janet L McLeod, et al.
Investigative Ophthalmology & Visual Science|June 30, 2004
Spectrum and frequency of FZD4 mutations in familial exudative vitreoretinopathyCarmel Toomes, Helen M Bottomley, Sheila Scott, et al.
European Journal of Human Genetics : EJHG|March 27, 2026
Non-coding structural variants disrupting conserved PITX2 enhancer loci in Axenfeld-Rieger syndromeLucas A Mitchell, Joshua Schmidt, Emmanuelle Souzeau, et al.
Ophthalmology|March 5, 2013
Higher prevalence of myocilin mutations in advanced glaucoma in comparison with less advanced disease in an Australasian disease registryEmmanuelle Souzeau, Kathryn P Burdon, Andrew Dubowsky, et al.
Plos One|October 11, 2012
The p53 codon 72 PRO/PRO genotype may be associated with initial central visual field defects in caucasians with primary open angle glaucomaJaney L Wiggs, Alex W Hewitt, Bao Jian Fan, et al.
Medrxiv : the Preprint Server for Health Sciences|June 12, 2025
Axenfeld-Rieger syndrome associated with a megabase-scale inversion separating <i>PITX2</i> from a conserved enhancer locusLucas A Mitchell, Joshua Schmidt, Emmanuelle Souzeau, et al.
Ophthalmology|October 30, 2007
Genetic dissection of myopia: evidence for linkage of ocular axial length to chromosome 5qGu Zhu, Alex W Hewitt, Jonathan B Ruddle, et al.
Human Mutation|May 11, 2021
A novel GSN variant outside the G2 calcium-binding domain associated with Amyloidosis of the Finnish typeSean Mullany, Emmanuelle Souzeau, Sonja Klebe, et al.
Pageof 36