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L J Hardwick

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

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Molecular and Cellular Probes|February 1, 1995
A simple method for rapid isolation of microsatellites from yeast artificial chromosomesJ Brown, L J Hardwick, A F Wright
Human Molecular Genetics|October 1, 1993
An STR polymorphism at the CYBB locusL J Hardwick, J Brown, A F Wright
Human Molecular Genetics|September 1, 1995
Linkage of the gene that encodes the alpha 1 chain of type V collagen (COL5A1) to type II Ehlers-Danlos syndrome (EDS II)J Loughlin, C Irven, L J Hardwick, et al.
Clinical Genetics|May 1, 1993
Linkage analysis in a family with complete type congenital stationary night blindness with and without myopiaK L Dry, D B Van Dorp, M A Aldred, et al.
The Journal of Rheumatology|January 1, 1997
Genetic mapping of susceptibility loci in the genes involved in rheumatoid arthritisL J Hardwick, S Walsh, S Butcher, et al.
American Journal of Human Genetics|July 1, 1994
Heterogeneity analysis in 40 X-linked retinitis pigmentosa familiesP W Teague, M A Aldred, M Jay, et al.
Human Molecular Genetics|December 1, 1995
Identification of a novel gene, ETX1 from Xp21.1, a candidate gene for X-linked retintis pigmentosa (RP3)K L Dry, M A Aldred, A J Edgar, et al.
Genomics|September 1, 1992
Linkage analysis in X-linked congenital stationary night blindnessM A Aldred, K L Dry, D M Sharp, et al.
American Journal of Human Genetics|November 1, 1994
Genetic analysis of a kindred with X-linked mental handicap and retinitis pigmentosaM A Aldred, K L Dry, E B Knight-Jones, et al.
Genomics|October 15, 1996
Analysis of three deletion breakpoints in Xp21.1 and the further localization of RP3J Brown, K L Dry, A J Edgar, et al.
Pageof 1

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

Sort By:
Pageof 1
Molecular and Cellular Probes|February 1, 1995
A simple method for rapid isolation of microsatellites from yeast artificial chromosomesJ Brown, L J Hardwick, A F Wright
Human Molecular Genetics|October 1, 1993
An STR polymorphism at the CYBB locusL J Hardwick, J Brown, A F Wright
Human Molecular Genetics|September 1, 1995
Linkage of the gene that encodes the alpha 1 chain of type V collagen (COL5A1) to type II Ehlers-Danlos syndrome (EDS II)J Loughlin, C Irven, L J Hardwick, et al.
Clinical Genetics|May 1, 1993
Linkage analysis in a family with complete type congenital stationary night blindness with and without myopiaK L Dry, D B Van Dorp, M A Aldred, et al.
The Journal of Rheumatology|January 1, 1997
Genetic mapping of susceptibility loci in the genes involved in rheumatoid arthritisL J Hardwick, S Walsh, S Butcher, et al.
American Journal of Human Genetics|July 1, 1994
Heterogeneity analysis in 40 X-linked retinitis pigmentosa familiesP W Teague, M A Aldred, M Jay, et al.
Human Molecular Genetics|December 1, 1995
Identification of a novel gene, ETX1 from Xp21.1, a candidate gene for X-linked retintis pigmentosa (RP3)K L Dry, M A Aldred, A J Edgar, et al.
Genomics|September 1, 1992
Linkage analysis in X-linked congenital stationary night blindnessM A Aldred, K L Dry, D M Sharp, et al.
American Journal of Human Genetics|November 1, 1994
Genetic analysis of a kindred with X-linked mental handicap and retinitis pigmentosaM A Aldred, K L Dry, E B Knight-Jones, et al.
Genomics|October 15, 1996
Analysis of three deletion breakpoints in Xp21.1 and the further localization of RP3J Brown, K L Dry, A J Edgar, et al.
Pageof 1