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Human Mutation|January 1, 1996
Mutations and polymorphisms in the human peripherin-RDS gene and their involvement in inherited retinal degenerationT J Keen, C F InglehearnCurrent Pharmaceutical Biotechnology|June 23, 2006
Does isoform diversity explain functional differences in the 14-3-3 protein family?E Kjarland, T J Keen, R KleppeJournal of Medical Genetics|February 1, 1997
Exclusion of CAG repeat expansion as the cause of disease in autosomal dominant retinitis pigmentosa familiesT J Keen, A G Morris, C F InglehearnGenomics|January 27, 1998
Analysis of a human gene homologous to rat ventral prostate.1 proteinR E Peacock, T J Keen, C F InglehearnAmerican Journal of Human Genetics|February 17, 2001
A new locus for autosomal dominant familial exudative vitreoretinopathy maps to chromosome 11p12-13L M Downey, T J Keen, E Roberts, et al.Human Molecular Genetics|April 1, 1992
A completed screen for mutations of the rhodopsin gene in a panel of patients with autosomal dominant retinitis pigmentosaC F Inglehearn, T J Keen, R Bashir, et al.Genomics|November 1, 1995
Regional assignment of 30 expressed sequence tags on human chromosome 7 using a somatic cell hybrid panelR J Patel, T J Keen, K H Grzeschik, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|April 1, 1995
Autosomal dominant pattern dystrophy of the retina associated with a 4-base pair insertion at codon 140 in the peripherin/RDS geneR Y Kim, H Dollfus, T J Keen, et al.Genomics|September 1, 1991
Autosomal dominant retinitis pigmentosa: four new mutations in rhodopsin, one of them in the retinal attachment siteT J Keen, C F Inglehearn, D H Lester, et al.Genes, Chromosomes & Cancer|November 1, 1996
Localization of a novel t(1;7) translocation associated with Wilms' tumor predisposition and skeletal abnormalitiesP A Reynolds, R M Powlesland, T J Keen, et al.Pageof 3