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H M Hammer

Showing results (11-20 of 18) with videos related to

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Investigative Ophthalmology & Visual Science|May 31, 2001
Spatial localization after different types of retinal detachment surgeryC R Weir, M Cleary, S Parks, et al.
Human Mutation|February 6, 1998
Rhodopsin splice site sequence changes in retinitis pigmentosa and their effect at the mRNA levelJ L Whitehead, C Bell, C A Converse, et al.
Eye (London, England)|July 9, 2002
Unilateral acute idiopathic maculopathy (UAIM) masquerading as Best's diseaseM R K Mathew, L A Webb, H G B Bennett, et al.
Journal of Medical Genetics|August 1, 1996
Linkage of a medium sized Scottish autosomal dominant retinitis pigmentosa family to chromosome 7qZ Mohamed, C Bell, H M Hammer, et al.
Ophthalmology|January 1, 1994
Pathology of hereditary retinal degeneration associated with hypobetalipoproteinemiaD M Brosnahan, S M Kennedy, C A Converse, et al.
Eye (London, England)|January 1, 1995
How much blame can be placed on laser photocoagulation for failure to attain driving standards?S W Mackie, L A Webb, B M Hutchison, et al.
Lipids|November 1, 1993
An increased incidence of apolipoprotein E2/E2 and E4/E4 in retinitis pigmentosaL Huq, T McLachlan, H M Hammer, et al.
Journal of Medical Genetics|November 1, 1989
Diagnostic and counselling difficulties using a fully comprehensive screening protocol for families at risk for tuberous sclerosisL I al-Gazali, R J Arthur, J T Lamb, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Investigative Ophthalmology & Visual Science|May 31, 2001
Spatial localization after different types of retinal detachment surgeryC R Weir, M Cleary, S Parks, et al.
Human Mutation|February 6, 1998
Rhodopsin splice site sequence changes in retinitis pigmentosa and their effect at the mRNA levelJ L Whitehead, C Bell, C A Converse, et al.
Eye (London, England)|July 9, 2002
Unilateral acute idiopathic maculopathy (UAIM) masquerading as Best's diseaseM R K Mathew, L A Webb, H G B Bennett, et al.
Journal of Medical Genetics|August 1, 1996
Linkage of a medium sized Scottish autosomal dominant retinitis pigmentosa family to chromosome 7qZ Mohamed, C Bell, H M Hammer, et al.
Ophthalmology|January 1, 1994
Pathology of hereditary retinal degeneration associated with hypobetalipoproteinemiaD M Brosnahan, S M Kennedy, C A Converse, et al.
Eye (London, England)|January 1, 1995
How much blame can be placed on laser photocoagulation for failure to attain driving standards?S W Mackie, L A Webb, B M Hutchison, et al.
Lipids|November 1, 1993
An increased incidence of apolipoprotein E2/E2 and E4/E4 in retinitis pigmentosaL Huq, T McLachlan, H M Hammer, et al.
Journal of Medical Genetics|November 1, 1989
Diagnostic and counselling difficulties using a fully comprehensive screening protocol for families at risk for tuberous sclerosisL I al-Gazali, R J Arthur, J T Lamb, et al.
Pageof 2