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D A Mackey

Showing results (51-60 of 65) with videos related to

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Clinical Genetics|January 31, 2012
A puzzle over several decades: eye anomalies with FRAS1 and STRA6 mutations in the same familyW Y Ng, F Pasutto, T M Bardakjian, et al.
Investigative Ophthalmology & Visual Science|January 3, 2001
Evaluation of the myocilin (MYOC) glaucoma gene in monkey and human steroid-induced ocular hypertensionJ H Fingert, A F Clark, J E Craig, et al.
The British Journal of Ophthalmology|June 21, 2005
The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genesJ D McKay, B Patterson, J E Craig, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|May 3, 2014
Multiple prenatal ultrasound scans and ocular development: 20-year follow-up of a randomized controlled trialH Forward, S Yazar, A W Hewitt, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 19, 2000
Accuracy and implications of a reported family history of glaucoma: experience from the Glaucoma Inheritance Study in TasmaniaA I McNaught, J G Allen, D L Healey, et al.
American Journal of Human Genetics|February 15, 2001
A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eyeD Y Nishimura, C C Searby, W L Alward, et al.
Ophthalmology|September 6, 2001
Evidence for genetic heterogeneity within eight glaucoma families, with the GLC1A Gln368STOP mutation being an important phenotypic modifierJ E Craig, P N Baird, D L Healey, et al.
The New England Journal of Medicine|April 16, 1998
Clinical features associated with mutations in the chromosome 1 open-angle glaucoma gene (GLC1A)W L Alward, J H Fingert, M A Coote, et al.
Ophthalmic Genetics|December 1, 1996
The problem of overlapping glaucoma families in the Glaucoma Inheritance Study in Tasmania (GIST)J Sack, D L Healey, A P de Graaf, et al.
Molecular Vision|August 19, 2011
Pediatric cataract, myopic astigmatism, familial exudative vitreoretinopathy and primary open-angle glaucoma co-segregating in a familyD A Mackey, A W Hewitt, J B Ruddle, et al.
Pageof 7

Showing results (51-60 of 65) with videos related to

Sort By:
Pageof 7
Clinical Genetics|January 31, 2012
A puzzle over several decades: eye anomalies with FRAS1 and STRA6 mutations in the same familyW Y Ng, F Pasutto, T M Bardakjian, et al.
Investigative Ophthalmology & Visual Science|January 3, 2001
Evaluation of the myocilin (MYOC) glaucoma gene in monkey and human steroid-induced ocular hypertensionJ H Fingert, A F Clark, J E Craig, et al.
The British Journal of Ophthalmology|June 21, 2005
The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genesJ D McKay, B Patterson, J E Craig, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|May 3, 2014
Multiple prenatal ultrasound scans and ocular development: 20-year follow-up of a randomized controlled trialH Forward, S Yazar, A W Hewitt, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 19, 2000
Accuracy and implications of a reported family history of glaucoma: experience from the Glaucoma Inheritance Study in TasmaniaA I McNaught, J G Allen, D L Healey, et al.
American Journal of Human Genetics|February 15, 2001
A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eyeD Y Nishimura, C C Searby, W L Alward, et al.
Ophthalmology|September 6, 2001
Evidence for genetic heterogeneity within eight glaucoma families, with the GLC1A Gln368STOP mutation being an important phenotypic modifierJ E Craig, P N Baird, D L Healey, et al.
The New England Journal of Medicine|April 16, 1998
Clinical features associated with mutations in the chromosome 1 open-angle glaucoma gene (GLC1A)W L Alward, J H Fingert, M A Coote, et al.
Ophthalmic Genetics|December 1, 1996
The problem of overlapping glaucoma families in the Glaucoma Inheritance Study in Tasmania (GIST)J Sack, D L Healey, A P de Graaf, et al.
Molecular Vision|August 19, 2011
Pediatric cataract, myopic astigmatism, familial exudative vitreoretinopathy and primary open-angle glaucoma co-segregating in a familyD A Mackey, A W Hewitt, J B Ruddle, et al.
Pageof 7