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G J Farrar

Showing results (1-10 of 47) with videos related to

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Nature Genetics|December 1, 1994
New dimensions in macular dystrophiesP Humphries, P Kenna, G J Farrar
Science (New York, N.Y.)|May 8, 1992
On the molecular genetics of retinitis pigmentosaP Humphries, P Kenna, G J Farrar
Clinical Genetics|July 1, 1990
Retinitis pigmentosa: genetic mapping in X-linked and autosomal forms of the diseaseP Humphries, G J Farrar, P Kenna, 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.
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.
Journal of Medical Genetics|February 25, 1998
Lack of evidence for genetic heterogeneity in Best vitelliform macular dystrophyF Mansergh, T Meitinger, G Rodolph, 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.
Nucleic Acids Research|October 25, 1991
Poly (T/A) polymorphism at the human retinal degeneration slow (RDS) locusR Kumar-Singh, S A Jordan, G J Farrar, et al.
Gene Therapy|November 18, 2011
Gene-based therapies for dominantly inherited retinopathiesG J Farrar, S Millington-Ward, N Chadderton, et al.
Nucleic Acids Research|December 25, 1991
A sequence polymorphism in the human peripherin/RDS geneG J Farrar, P Kenna, S A Jordan, et al.
Pageof 5

Showing results (1-10 of 47) with videos related to

Sort By:
Pageof 5
Nature Genetics|December 1, 1994
New dimensions in macular dystrophiesP Humphries, P Kenna, G J Farrar
Science (New York, N.Y.)|May 8, 1992
On the molecular genetics of retinitis pigmentosaP Humphries, P Kenna, G J Farrar
Clinical Genetics|July 1, 1990
Retinitis pigmentosa: genetic mapping in X-linked and autosomal forms of the diseaseP Humphries, G J Farrar, P Kenna, 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.
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.
Journal of Medical Genetics|February 25, 1998
Lack of evidence for genetic heterogeneity in Best vitelliform macular dystrophyF Mansergh, T Meitinger, G Rodolph, 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.
Nucleic Acids Research|October 25, 1991
Poly (T/A) polymorphism at the human retinal degeneration slow (RDS) locusR Kumar-Singh, S A Jordan, G J Farrar, et al.
Gene Therapy|November 18, 2011
Gene-based therapies for dominantly inherited retinopathiesG J Farrar, S Millington-Ward, N Chadderton, et al.
Nucleic Acids Research|December 25, 1991
A sequence polymorphism in the human peripherin/RDS geneG J Farrar, P Kenna, S A Jordan, et al.
Pageof 5