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Neuromuscular Disorders : NMD|July 1, 1997
Improved adenoviral vectors for gene therapy of Duchenne muscular dystrophyM A Hauser, A Amalfitano, R Kumar-Singh, et al.Human Molecular Genetics|July 1, 1993
Exclusion of the involvement of all known retinitis pigmentosa loci in the disease present in a family of Irish origin provides evidence for a sixth autosomal dominant locus (RP8)R Kumar-Singh, G J Farrar, F Mansergh, et al.Human Genetics|March 1, 1991
Autosomal dominant retinitis pigmentosa: a new multi-allelic marker (D3S621) genetically linked to the disease locus (RP4)R Kumar-Singh, D G Bradley, G J Farrar, et al.The British Journal of Ophthalmology|March 1, 1997
Clinical and molecular genetic characterisation of a family segregating autosomal dominant retinitis pigmentosa and sensorineural deafnessP Kenna, F Mansergh, S Millington-Ward, et al.Genomics|November 1, 1992
Autosomal dominant retinitis pigmentosa: a novel mutation at the peripherin/RDS locus in the original 6p-linked pedigreeG J Farrar, P Kenna, S A Jordan, et al.American Journal of Human Genetics|March 1, 1992
Autosomal dominant retinitis pigmentosa (adRP; RP6): cosegregation of RP6 and the peripherin-RDS locus in a late-onset family of Irish originS A Jordan, G J Farrar, R Kumar-Singh, et al.Nature|December 12, 1991
A three-base-pair deletion in the peripherin-RDS gene in one form of retinitis pigmentosaG J Farrar, P Kenna, S A Jordan, et al.Genomics|December 1, 1991
Autosomal dominant retinitis pigmentosa: localization of a disease gene (RP6) to the short arm of chromosome 6G J Farrar, S A Jordan, P Kenna, et al.Human Mutation|January 1, 1993
A mutation (Met-->Arg) in the type I keratin (K14) gene responsible for autosomal dominant epidermolysis bullosa simplexM M Humphries, D M Sheils, G J Farrar, et al.Nature Genetics|May 1, 1993
Localization of an autosomal dominant retinitis pigmentosa gene to chromosome 7qS A Jordan, G J Farrar, P Kenna, et al.Pageof 3