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J R Yates

Showing results (121-130 of 227) with videos related to

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Clinical and Experimental Dermatology|July 1, 1997
Genetic linkage to the collagen alpha 1 (V) gene (COL5A1) in two British Ehlers-Danlos syndrome families with variable type I and II phenotypesN P Burrows, A C Nicholls, J R Yates, et al.
Advances in Dental Research|September 16, 2011
Scientific frontiers: emerging technologies for salivary diagnosticsB J Baum, J R Yates, S Srivastava, et al.
The British Journal of Ophthalmology|April 1, 1993
Clinical features of affected males with X linked ocular albinismS J Charles, J S Green, J W Grant, et al.
Journal of Physics. Condensed Matter : an Institute of Physics Journal|October 31, 2013
Oxygen K-edge electron energy loss spectra of hydrous and anhydrous compoundsB Winkler, M Avalos-Borja, V Milman, et al.
European Journal of Human Genetics : EJHG|November 26, 1999
Stickler syndrome: further mutations in COL11A1 and evidence for additional locus heterogeneityS Martin, A J Richards, J R Yates, et al.
Journal of Medical Genetics|September 1, 1987
Linkage of the tuberous sclerosis locus to a DNA polymorphism detected by v-ablJ M Connor, L A Pirrit, J R Yates, et al.
Journal of Medical Genetics|November 14, 1997
Instability of normal (CTG)n alleles in the DM kinase geneD J Dow, D C Rubinsztein, J R Yates, et al.
Human Genetics|July 8, 1999
Exclusion of RAI2 as the causative gene for Nance-Horan syndromeS M Walpole, N Ronce, C Grayson, et al.
Neuromuscular Disorders : NMD|July 10, 1999
A protein truncation test for Emery-Dreifuss muscular dystrophy (EMD): detection of N-terminal truncating mutationsP A de Koning Gans, I Ginjaar, E Bakker, et al.
Human Genetics|January 1, 1985
Multipoint linkage analysis of the short arm of the human X chromosome in families with X-linked muscular dystrophyD E Wilcox, N A Affara, J R Yates, et al.
Pageof 23

Showing results (121-130 of 227) with videos related to

Sort By:
Pageof 23
Clinical and Experimental Dermatology|July 1, 1997
Genetic linkage to the collagen alpha 1 (V) gene (COL5A1) in two British Ehlers-Danlos syndrome families with variable type I and II phenotypesN P Burrows, A C Nicholls, J R Yates, et al.
Advances in Dental Research|September 16, 2011
Scientific frontiers: emerging technologies for salivary diagnosticsB J Baum, J R Yates, S Srivastava, et al.
The British Journal of Ophthalmology|April 1, 1993
Clinical features of affected males with X linked ocular albinismS J Charles, J S Green, J W Grant, et al.
Journal of Physics. Condensed Matter : an Institute of Physics Journal|October 31, 2013
Oxygen K-edge electron energy loss spectra of hydrous and anhydrous compoundsB Winkler, M Avalos-Borja, V Milman, et al.
European Journal of Human Genetics : EJHG|November 26, 1999
Stickler syndrome: further mutations in COL11A1 and evidence for additional locus heterogeneityS Martin, A J Richards, J R Yates, et al.
Journal of Medical Genetics|September 1, 1987
Linkage of the tuberous sclerosis locus to a DNA polymorphism detected by v-ablJ M Connor, L A Pirrit, J R Yates, et al.
Journal of Medical Genetics|November 14, 1997
Instability of normal (CTG)n alleles in the DM kinase geneD J Dow, D C Rubinsztein, J R Yates, et al.
Human Genetics|July 8, 1999
Exclusion of RAI2 as the causative gene for Nance-Horan syndromeS M Walpole, N Ronce, C Grayson, et al.
Neuromuscular Disorders : NMD|July 10, 1999
A protein truncation test for Emery-Dreifuss muscular dystrophy (EMD): detection of N-terminal truncating mutationsP A de Koning Gans, I Ginjaar, E Bakker, et al.
Human Genetics|January 1, 1985
Multipoint linkage analysis of the short arm of the human X chromosome in families with X-linked muscular dystrophyD E Wilcox, N A Affara, J R Yates, et al.
Pageof 23