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C E Willoughby

Showing results (1-10 of 14) with videos related to

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Eye (London, England)|October 17, 1998
The presence of congenital hypertrophy of the retinal pigment epithelium in a subgroup of patients with adenomatous polyposis coli mutationsC E Willoughby
Eye (London, England)|October 1, 2011
A mutation in the Norrie disease gene (NDP) associated with familial exudative vitreoretinopathyS Chamney, E McLoone, C E Willoughby
Eye (London, England)|January 1, 1993
Assessment of the value of congenital hypertrophy of the retinal pigment epithelium as an ocular marker for familial adenomatous polyposis coliM U Hickey-Dwyer, C E Willoughby
Survey of Ophthalmology|March 29, 2002
Collagen corneal shieldsC E Willoughby, M Batterbury, S B Kaye
Biology of Reproduction|September 1, 1996
Osmotic tolerance limits and properties of murine spermatozoaC E Willoughby, P Mazur, A T Peter, et al.
Eye (London, England)|October 17, 2015
The ocular phenotype of stiff-skin syndromeS Chamney, B Cartmill, O Earley, et al.
Eye (London, England)|April 22, 2008
Ocular manifestations in oculodentodigital dysplasia resulting from a heterozygous missense mutation (L113P) in GJA1 (connexin 43)F U Musa, P Ratajczak, J Sahu, et al.
Biology of Reproduction|September 24, 1999
Effects of Percoll separation, cryoprotective agents, and temperature on plasma membrane permeability characteristics of murine spermatozoa and their relevance to cryopreservationM J Phelps, J Liu, J D Benson, et al.
Journal of Medical Genetics|November 25, 2003
A novel GJA8 mutation in an Iranian family with progressive autosomal dominant congenital nuclear cataractC E Willoughby, Sara Arab, R Gandhi, et al.
Journal of Medical Virology|September 13, 2002
Epstein-Barr virus (types 1 and 2) in the tear film in Sjogren's syndrome and HIV infectionC E Willoughby, K Baker, S B Kaye, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Eye (London, England)|October 17, 1998
The presence of congenital hypertrophy of the retinal pigment epithelium in a subgroup of patients with adenomatous polyposis coli mutationsC E Willoughby
Eye (London, England)|October 1, 2011
A mutation in the Norrie disease gene (NDP) associated with familial exudative vitreoretinopathyS Chamney, E McLoone, C E Willoughby
Eye (London, England)|January 1, 1993
Assessment of the value of congenital hypertrophy of the retinal pigment epithelium as an ocular marker for familial adenomatous polyposis coliM U Hickey-Dwyer, C E Willoughby
Survey of Ophthalmology|March 29, 2002
Collagen corneal shieldsC E Willoughby, M Batterbury, S B Kaye
Biology of Reproduction|September 1, 1996
Osmotic tolerance limits and properties of murine spermatozoaC E Willoughby, P Mazur, A T Peter, et al.
Eye (London, England)|October 17, 2015
The ocular phenotype of stiff-skin syndromeS Chamney, B Cartmill, O Earley, et al.
Eye (London, England)|April 22, 2008
Ocular manifestations in oculodentodigital dysplasia resulting from a heterozygous missense mutation (L113P) in GJA1 (connexin 43)F U Musa, P Ratajczak, J Sahu, et al.
Biology of Reproduction|September 24, 1999
Effects of Percoll separation, cryoprotective agents, and temperature on plasma membrane permeability characteristics of murine spermatozoa and their relevance to cryopreservationM J Phelps, J Liu, J D Benson, et al.
Journal of Medical Genetics|November 25, 2003
A novel GJA8 mutation in an Iranian family with progressive autosomal dominant congenital nuclear cataractC E Willoughby, Sara Arab, R Gandhi, et al.
Journal of Medical Virology|September 13, 2002
Epstein-Barr virus (types 1 and 2) in the tear film in Sjogren's syndrome and HIV infectionC E Willoughby, K Baker, S B Kaye, et al.
Pageof 2