R Kumar-Singh|S A Jordan|G J Farrar|P Humphries - JoVE Visualize

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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.

American Journal of Human Genetics|February 1, 1993

Autosomal dominant retinitis pigmentosa: no evidence for nonallelic genetic heterogeneity on 3qR Kumar-Singh, H Wang, P Humphries, et al.

Genomics|January 1, 1993

Evidence for further genetic heterogeneity in autosomal dominant retinitis pigmentosaR Kumar-Singh, P F Kenna, G J Farrar, et al.

Human Mutation|January 1, 1992

Polymorphic variation within "conserved" sequences at the 3' end of the human RDS gene which results in amino acid substitutionsS A Jordan, G J Farrar, P Kenna, 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.

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.

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Showing results (1-10 of 159) with videos related to

Sort By:

Pageof 16

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.

American Journal of Human Genetics|February 1, 1993

Autosomal dominant retinitis pigmentosa: no evidence for nonallelic genetic heterogeneity on 3qR Kumar-Singh, H Wang, P Humphries, et al.

Genomics|January 1, 1993

Evidence for further genetic heterogeneity in autosomal dominant retinitis pigmentosaR Kumar-Singh, P F Kenna, G J Farrar, et al.

Human Mutation|January 1, 1992

Polymorphic variation within "conserved" sequences at the 3' end of the human RDS gene which results in amino acid substitutionsS A Jordan, G J Farrar, P Kenna, 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.

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.

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