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BJU International
|
November 9, 2000
Current status of linkage studies in hereditary prostate cancer
M K Karayi, D E Neal, A F Markham
The Journal of Biological Chemistry
|
July 10, 1983
Isolation of a cDNA clone for human antithrombin III
E V Prochownik, A F Markham, S H Orkin
Thrombosis and Haemostasis
|
November 1, 2000
Factor XIII deficiency causing mutation, Ser295Arg, in exon 7 of the factor XIIIA gene
R Anwar, L Gallivan, K J Miloszewski, et al.
Human Genetics
|
March 1, 1991
The human aldose reductase gene maps to chromosome region 7q35
A Graham, P Heath, J E Morten, et al.
Nucleic Acids Research
|
October 25, 1989
Rapid determination of DNA concentration in multiple samples
J Riley, D Jenner, J C Smith, et al.
Clinical Molecular Pathology
|
October 1, 1996
Novel primer specific false terminations during DNA sequencing reactions: danger of inaccuracy of mutation analysis in molecular diagnostics
R Anwar, A Booth, A J Churchill, et al.
British Journal of Haematology
|
November 25, 1998
Splicing and missense mutations in the human FXIIIA gene causing FXIII deficiency: effects of these mutations on FXIIIA RNA processing and protein structure
R Anwar, L Gallivan, K J Miloszewski, et al.
Blood
|
January 28, 1999
Genotype/phenotype correlations for coagulation factor XIII: specific normal polymorphisms are associated with high or low factor XIII specific activity
R Anwar, L Gallivan, S D Edmonds, et al.
Nature
|
July 3, 1983
mRNA sequences define an unusually restricted IgG response to 2-phenyloxazolone and its early diversification
M Kaartinen, G M Griffiths, A F Markham, et al.
Genomics
|
June 1, 1992
A human aldehyde dehydrogenase (aldose reductase) pseudogene: nucleotide sequence analysis and assignment to chromosome 3
L Brown, P J Hedge, A F Markham, et al.
Page
of 24
Search research articles
Search
Showing results (31-40 of 231) with videos related to
Sort By:
Page
of 24
BJU International
|
November 9, 2000
Current status of linkage studies in hereditary prostate cancer
M K Karayi, D E Neal, A F Markham
The Journal of Biological Chemistry
|
July 10, 1983
Isolation of a cDNA clone for human antithrombin III
E V Prochownik, A F Markham, S H Orkin
Thrombosis and Haemostasis
|
November 1, 2000
Factor XIII deficiency causing mutation, Ser295Arg, in exon 7 of the factor XIIIA gene
R Anwar, L Gallivan, K J Miloszewski, et al.
Human Genetics
|
March 1, 1991
The human aldose reductase gene maps to chromosome region 7q35
A Graham, P Heath, J E Morten, et al.
Nucleic Acids Research
|
October 25, 1989
Rapid determination of DNA concentration in multiple samples
J Riley, D Jenner, J C Smith, et al.
Clinical Molecular Pathology
|
October 1, 1996
Novel primer specific false terminations during DNA sequencing reactions: danger of inaccuracy of mutation analysis in molecular diagnostics
R Anwar, A Booth, A J Churchill, et al.
British Journal of Haematology
|
November 25, 1998
Splicing and missense mutations in the human FXIIIA gene causing FXIII deficiency: effects of these mutations on FXIIIA RNA processing and protein structure
R Anwar, L Gallivan, K J Miloszewski, et al.
Blood
|
January 28, 1999
Genotype/phenotype correlations for coagulation factor XIII: specific normal polymorphisms are associated with high or low factor XIII specific activity
R Anwar, L Gallivan, S D Edmonds, et al.
Nature
|
July 3, 1983
mRNA sequences define an unusually restricted IgG response to 2-phenyloxazolone and its early diversification
M Kaartinen, G M Griffiths, A F Markham, et al.
Genomics
|
June 1, 1992
A human aldehyde dehydrogenase (aldose reductase) pseudogene: nucleotide sequence analysis and assignment to chromosome 3
L Brown, P J Hedge, A F Markham, et al.
Page
of 24