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Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie
|
September 16, 1999
Familial occurrence of pseudoexfoliation in Canada
K F Damji, H S Bains, K Amjadi, et al.
The British Journal of Ophthalmology
|
May 5, 2006
Intraocular pressure following phacoemulsification in patients with and without exfoliation syndrome: a 2 year prospective study
K F Damji, A G P Konstas, J M Liebmann, et al.
Archives of Neurology
|
April 1, 1996
Periodic vestibulocerebellar ataxia, an autosomal dominant ataxia with defective smooth pursuit, is genetically distinct from other autosomal dominant ataxias
K F Damji, R R Allingham, S C Pollock, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie
|
September 8, 2001
Leber's congenital amaurosis with anterior keratoconus in Pakistani families is caused by the Trp278X mutation in the AIPL1 gene on 17p
K F Damji, M M Sohocki, R Khan, et al.
Human Genetics
|
April 1, 1998
Quantitative DNA pooling to increase the efficiency of linkage analysis in autosomal dominant disease
K F Damji, C J Gallione, R R Allingham, et al.
Human Heredity
|
September 28, 1998
Adult-onset primary open angle glaucoma does not localize to chromosome 2cen-q13 in North American families
R R Allingham, J L Wiggs, K F Damji, et al.
Page
of 5
Search research articles
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Showing results (41-50 of 46) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 46 results.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie
|
September 16, 1999
Familial occurrence of pseudoexfoliation in Canada
K F Damji, H S Bains, K Amjadi, et al.
The British Journal of Ophthalmology
|
May 5, 2006
Intraocular pressure following phacoemulsification in patients with and without exfoliation syndrome: a 2 year prospective study
K F Damji, A G P Konstas, J M Liebmann, et al.
Archives of Neurology
|
April 1, 1996
Periodic vestibulocerebellar ataxia, an autosomal dominant ataxia with defective smooth pursuit, is genetically distinct from other autosomal dominant ataxias
K F Damji, R R Allingham, S C Pollock, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie
|
September 8, 2001
Leber's congenital amaurosis with anterior keratoconus in Pakistani families is caused by the Trp278X mutation in the AIPL1 gene on 17p
K F Damji, M M Sohocki, R Khan, et al.
Human Genetics
|
April 1, 1998
Quantitative DNA pooling to increase the efficiency of linkage analysis in autosomal dominant disease
K F Damji, C J Gallione, R R Allingham, et al.
Human Heredity
|
September 28, 1998
Adult-onset primary open angle glaucoma does not localize to chromosome 2cen-q13 in North American families
R R Allingham, J L Wiggs, K F Damji, et al.
Page
of 5