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Genetic Testing
|
August 23, 2000
Geography of HFE C282Y and H63D mutations
A 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 hydroxylase
S 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 implications
C 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 phenylketonuria
J 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 mutation
A 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 dystrophies
S 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 falciparum
S Krishna, G Cowan, J C Meade, et al.
Physics in Medicine and Biology
|
December 9, 2004
Mammographic image restoration using maximum entropy deconvolution
A Jannetta, J C Jackson, C J Kotre, et al.
Biochemistry
|
November 20, 1984
Sequence comparison of rat liver phenylalanine hydroxylase and its cDNA clones
K 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 clones
M L Snead, M Zeichner-David, T Chandra, et al.
Page
of 9
Search research articles
Search
Showing results (51-60 of 85) with videos related to
Sort By:
Page
of 9
Genetic Testing
|
August 23, 2000
Geography of HFE C282Y and H63D mutations
A 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 hydroxylase
S 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 implications
C 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 phenylketonuria
J 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 mutation
A 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 dystrophies
S 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 falciparum
S Krishna, G Cowan, J C Meade, et al.
Physics in Medicine and Biology
|
December 9, 2004
Mammographic image restoration using maximum entropy deconvolution
A Jannetta, J C Jackson, C J Kotre, et al.
Biochemistry
|
November 20, 1984
Sequence comparison of rat liver phenylalanine hydroxylase and its cDNA clones
K 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 clones
M L Snead, M Zeichner-David, T Chandra, et al.
Page
of 9