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Proceedings of the National Academy of Sciences of the United States of America|August 4, 1999
Biochemical analysis of a dimerization domain mutation in RetGC-1 associated with dominant cone-rod dystrophyC L Tucker, S C Woodcock, R E Kelsell, et al.
British Journal of Haematology|November 1, 1980
The genetic basis of Hb Q-H diseaseD R Higgs, D M Hunt, H C Drysdale, et al.
Human Molecular Genetics|April 1, 1997
Localisation of a gene for dominant cone-rod dystrophy (CORD6) to chromosome 17pR E Kelsell, K Evans, C Y Gregory, et al.
Biochemistry|July 13, 2000
Spectral tuning of avian violet- and ultraviolet-sensitive visual pigmentsS E Wilkie, P R Robinson, T W Cronin, et al.
Schizophrenia Research|May 24, 1997
The number of triplet repeats in five brain-expressed loci with CAG repeats is not associated with schizophreniaE J Gaitonde, S Sivagnanasundaram, A G Morris, et al.
Gene Therapy|May 18, 1999
Immune responses limit adenovirally mediated gene expression in the adult mouse eyeM B Reichel, R R Ali, A J Thrasher, et al.
The British Journal of Ophthalmology|January 25, 2005
A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1M Michaelides, G E Holder, D M Hunt, et al.
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