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M M Humphries

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Cytogenetics and Cell Genetics|January 1, 1989
Linkage analysis of human chromosome 4: exclusion of autosomal dominant retinitis pigmentosa (ADRP) and detection of new linkage groupsS P Daiger, M M Humphries, N Giesenschlag, et al.
Human Molecular Genetics|June 17, 1999
Structural and functional rescue of murine rod photoreceptors by human rhodopsin transgeneN McNally, P Kenna, M M Humphries, et al.
American Journal of Human Genetics|April 1, 1989
Autosomal dominant retinitis pigmentosa: exclusion of the gene from the short arm of chromosome 1 including the region surrounding the rhesus locusD G Bradley, G J Farrar, E M Sharp, 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.
Genomics|October 1, 1989
Autosomal dominant retinitis pigmentosa (ADRP): localization of an ADRP gene to the long arm of chromosome 3P McWilliam, G J Farrar, P Kenna, et al.
American Journal of Human Genetics|December 1, 1990
Autosomal dominant retinitis pigmentosa: absence of the rhodopsin proline----histidine substitution (codon 23) in pedigrees from EuropeG J Farrar, P Kenna, R Redmond, et al.
Genomics|July 1, 1990
Epidermolysis bullosa: evidence for linkage to genetic markers on chromosome 1 in a family with the autosomal dominant simplex formM M Humphries, D Sheils, M Lawler, et al.
Genomics|September 1, 1990
Autosomal dominant retinitis pigmentosa: linkage to rhodopsin and evidence for genetic heterogeneityG J Farrar, P McWilliam, D G Bradley, 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.
Journal of Medical Genetics|November 1, 1995
Evidence for genetic heterogeneity in Best's vitelliform macular dystrophyF C Mansergh, P F Kenna, G Rudolph, et al.
Pageof 4

Showing results (21-30 of 35) with videos related to

Sort By:
Pageof 4
Cytogenetics and Cell Genetics|January 1, 1989
Linkage analysis of human chromosome 4: exclusion of autosomal dominant retinitis pigmentosa (ADRP) and detection of new linkage groupsS P Daiger, M M Humphries, N Giesenschlag, et al.
Human Molecular Genetics|June 17, 1999
Structural and functional rescue of murine rod photoreceptors by human rhodopsin transgeneN McNally, P Kenna, M M Humphries, et al.
American Journal of Human Genetics|April 1, 1989
Autosomal dominant retinitis pigmentosa: exclusion of the gene from the short arm of chromosome 1 including the region surrounding the rhesus locusD G Bradley, G J Farrar, E M Sharp, 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.
Genomics|October 1, 1989
Autosomal dominant retinitis pigmentosa (ADRP): localization of an ADRP gene to the long arm of chromosome 3P McWilliam, G J Farrar, P Kenna, et al.
American Journal of Human Genetics|December 1, 1990
Autosomal dominant retinitis pigmentosa: absence of the rhodopsin proline----histidine substitution (codon 23) in pedigrees from EuropeG J Farrar, P Kenna, R Redmond, et al.
Genomics|July 1, 1990
Epidermolysis bullosa: evidence for linkage to genetic markers on chromosome 1 in a family with the autosomal dominant simplex formM M Humphries, D Sheils, M Lawler, et al.
Genomics|September 1, 1990
Autosomal dominant retinitis pigmentosa: linkage to rhodopsin and evidence for genetic heterogeneityG J Farrar, P McWilliam, D G Bradley, 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.
Journal of Medical Genetics|November 1, 1995
Evidence for genetic heterogeneity in Best's vitelliform macular dystrophyF C Mansergh, P F Kenna, G Rudolph, et al.
Pageof 4