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G R Standen

Showing results (1-10 of 49) with videos related to

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Journal of the Royal College of Physicians of London|April 1, 1988
Wiskott-Aldrich syndrome: new perspectives in pathogenesis and managementG R Standen
Journal of Clinical Pathology|December 1, 1991
Wiskott-Aldrich syndrome: a multidisciplinary diseaseG R Standen
Thrombosis and Haemostasis|May 1, 1995
Molecular analysis in factor XIIIA deficiencyS Aslam, G R Standen
Cancer Genetics and Cytogenetics|August 1, 1993
Wiskott-Aldrich syndrome: no evidence of chromosome instabilityP Thompson, G R Standen
Postgraduate Medical Journal|November 28, 1997
Rapid diagnosis of asymptomatic hereditary haemochromatosis by detection of the Cys282Tyr mutation in the HLA-H geneS Aslam, G R Standen
Acta Haematologica|January 1, 1980
Effect of daily administration of cytotoxic drugs on the erythroid and granulocytic repopulating ability of rat bone marrowG R Standen, N M Blackett
British Journal of Haematology|April 28, 2001
Heterozygosity for the thiopurine methyltransferase *3A allele in an acute non-lymphoblastic leukaemia patient with delayed marrow regeneration following H-DAT chemotherapyG R Standen, N A Wood
British Journal of Haematology|December 1, 1993
Factor XIII ABristol 1: detection of a nonsense mutation (Arg171-->stop codon) in factor XIII A subunit deficiencyG R Standen, D J Bowen
The Quarterly Journal of Medicine|May 1, 1991
The molecular biology of von Willebrand's diseaseG R Standen, I R Peake
British Journal of Haematology|June 1, 1997
Genetic detection of factor V Leiden: the question of specificityD J Bowen, G R Standen
Pageof 5

Showing results (1-10 of 49) with videos related to

Sort By:
Pageof 5
Journal of the Royal College of Physicians of London|April 1, 1988
Wiskott-Aldrich syndrome: new perspectives in pathogenesis and managementG R Standen
Journal of Clinical Pathology|December 1, 1991
Wiskott-Aldrich syndrome: a multidisciplinary diseaseG R Standen
Thrombosis and Haemostasis|May 1, 1995
Molecular analysis in factor XIIIA deficiencyS Aslam, G R Standen
Cancer Genetics and Cytogenetics|August 1, 1993
Wiskott-Aldrich syndrome: no evidence of chromosome instabilityP Thompson, G R Standen
Postgraduate Medical Journal|November 28, 1997
Rapid diagnosis of asymptomatic hereditary haemochromatosis by detection of the Cys282Tyr mutation in the HLA-H geneS Aslam, G R Standen
Acta Haematologica|January 1, 1980
Effect of daily administration of cytotoxic drugs on the erythroid and granulocytic repopulating ability of rat bone marrowG R Standen, N M Blackett
British Journal of Haematology|April 28, 2001
Heterozygosity for the thiopurine methyltransferase *3A allele in an acute non-lymphoblastic leukaemia patient with delayed marrow regeneration following H-DAT chemotherapyG R Standen, N A Wood
British Journal of Haematology|December 1, 1993
Factor XIII ABristol 1: detection of a nonsense mutation (Arg171-->stop codon) in factor XIII A subunit deficiencyG R Standen, D J Bowen
The Quarterly Journal of Medicine|May 1, 1991
The molecular biology of von Willebrand's diseaseG R Standen, I R Peake
British Journal of Haematology|June 1, 1997
Genetic detection of factor V Leiden: the question of specificityD J Bowen, G R Standen
Pageof 5