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K J Robson

Showing results (51-60 of 85) with videos related to

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Genetic Testing|August 23, 2000
Geography of HFE C282Y and H63D mutationsA T Merryweather-Clarke, J J Pointon, A M Jouanolle, et al.
Biochemistry|January 29, 1985
Nucleotide sequence of a full-length complementary DNA clone and amino acid sequence of human phenylalanine hydroxylaseS C Kwok, F D Ledley, A G DiLella, et al.
The British Journal of Radiology|July 9, 2004
Application of low dose rate pulsed fluoroscopy in cardiac pacing and electrophysiology: patient dose and image quality implicationsC J Kotre, S Charlton, K J Robson, et al.
Nucleic Acids Research|July 24, 1987
GT to AT transition at a splice donor site causes skipping of the preceding exon in phenylketonuriaJ Marvit, A G DiLella, K Brayton, et al.
British Journal of Haematology|December 31, 1997
A rapid non-invasive method for the detection of the haemochromatosis C282Y mutationA T Merryweather-Clarke, Y T Liu, J D Shearman, et al.
Genomics|February 1, 1988
Further studies of gene deletions that cause Duchenne and Becker muscular dystrophiesS M Forrest, G S Cross, T Flint, et al.
The Journal of Cell Biology|January 1, 1993
A family of cation ATPase-like molecules from Plasmodium falciparumS Krishna, G Cowan, J C Meade, et al.
Physics in Medicine and Biology|December 9, 2004
Mammographic image restoration using maximum entropy deconvolutionA Jannetta, J C Jackson, C J Kotre, et al.
Biochemistry|November 20, 1984
Sequence comparison of rat liver phenylalanine hydroxylase and its cDNA clonesK J Robson, W Beattie, R J James, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1983
Construction and identification of mouse amelogenin cDNA clonesM L Snead, M Zeichner-David, T Chandra, et al.
Pageof 9

Showing results (51-60 of 85) with videos related to

Sort By:
Pageof 9
Genetic Testing|August 23, 2000
Geography of HFE C282Y and H63D mutationsA T Merryweather-Clarke, J J Pointon, A M Jouanolle, et al.
Biochemistry|January 29, 1985
Nucleotide sequence of a full-length complementary DNA clone and amino acid sequence of human phenylalanine hydroxylaseS C Kwok, F D Ledley, A G DiLella, et al.
The British Journal of Radiology|July 9, 2004
Application of low dose rate pulsed fluoroscopy in cardiac pacing and electrophysiology: patient dose and image quality implicationsC J Kotre, S Charlton, K J Robson, et al.
Nucleic Acids Research|July 24, 1987
GT to AT transition at a splice donor site causes skipping of the preceding exon in phenylketonuriaJ Marvit, A G DiLella, K Brayton, et al.
British Journal of Haematology|December 31, 1997
A rapid non-invasive method for the detection of the haemochromatosis C282Y mutationA T Merryweather-Clarke, Y T Liu, J D Shearman, et al.
Genomics|February 1, 1988
Further studies of gene deletions that cause Duchenne and Becker muscular dystrophiesS M Forrest, G S Cross, T Flint, et al.
The Journal of Cell Biology|January 1, 1993
A family of cation ATPase-like molecules from Plasmodium falciparumS Krishna, G Cowan, J C Meade, et al.
Physics in Medicine and Biology|December 9, 2004
Mammographic image restoration using maximum entropy deconvolutionA Jannetta, J C Jackson, C J Kotre, et al.
Biochemistry|November 20, 1984
Sequence comparison of rat liver phenylalanine hydroxylase and its cDNA clonesK J Robson, W Beattie, R J James, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1983
Construction and identification of mouse amelogenin cDNA clonesM L Snead, M Zeichner-David, T Chandra, et al.
Pageof 9