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G R Standen

Showing results (31-40 of 49) with videos related to

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Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 26, 1998
A novel insertion mutation (1286insC) in exon 9 of the factor XIII-A subunit geneS Aslam, G R Standen, L J Bruce, et al.
International Journal of Cell Cloning|July 1, 1987
Production of hemopoietic growth factors and gamma-interferon by large granular lymphocytes from patients with T gamma lymphocytosisG R Standen, G Masters, R Pill, et al.
The British Journal of Dermatology|May 20, 2003
Idiopathic hypereosinophilic syndrome associated with cutaneous infarction and deep venous thrombosisS Narayan, F Ezughah, G R Standen, et al.
British Journal of Haematology|October 1, 1995
Factor XIIIA Calgary: a candidate missense mutation (Leu667Pro) in the beta barrel 2 domain of the factor XIIIA subunitS Aslam, M C Poon, V C Yee, et al.
British Journal of Haematology|October 1, 1990
Family studies in von Willebrand's disease by analysis of restriction fragment length polymorphisms and an intragenic variable number tandem repeat (VNTR) sequenceG R Standen, P Bignell, D J Bowen, et al.
The British Journal of Dermatology|May 16, 2000
Cutaneous presentation of steroid responsive blastoid natural killer cell lymphomaC P Bower, G R Standen, J Pawade, et al.
Blood|November 5, 1997
Identification of T-cell epitopes on the Rhesus polypeptides in autoimmune hemolytic anemiaR N Barker, A M Hall, G R Standen, et al.
Lancet (London, England)|September 8, 1990
Rapid neonatal diagnosis of von Willebrand's disease by use of the polymerase chain reactionP Bignell, G R Standen, D J Bowen, et al.
Thrombosis and Haemostasis|January 1, 1997
Genetic diagnosis of factor V Leiden using heteroduplex technologyD J Bowen, G R Standen, S Granville, et al.
American Journal of Hematology|August 1, 1989
Myelodysplastic syndrome with trisomy 8 in an adolescent with Fanconi anaemia and selective IgA deficiencyG R Standen, I A Hughes, A D Geddes, et al.
Pageof 5

Showing results (31-40 of 49) with videos related to

Sort By:
Pageof 5
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 26, 1998
A novel insertion mutation (1286insC) in exon 9 of the factor XIII-A subunit geneS Aslam, G R Standen, L J Bruce, et al.
International Journal of Cell Cloning|July 1, 1987
Production of hemopoietic growth factors and gamma-interferon by large granular lymphocytes from patients with T gamma lymphocytosisG R Standen, G Masters, R Pill, et al.
The British Journal of Dermatology|May 20, 2003
Idiopathic hypereosinophilic syndrome associated with cutaneous infarction and deep venous thrombosisS Narayan, F Ezughah, G R Standen, et al.
British Journal of Haematology|October 1, 1995
Factor XIIIA Calgary: a candidate missense mutation (Leu667Pro) in the beta barrel 2 domain of the factor XIIIA subunitS Aslam, M C Poon, V C Yee, et al.
British Journal of Haematology|October 1, 1990
Family studies in von Willebrand's disease by analysis of restriction fragment length polymorphisms and an intragenic variable number tandem repeat (VNTR) sequenceG R Standen, P Bignell, D J Bowen, et al.
The British Journal of Dermatology|May 16, 2000
Cutaneous presentation of steroid responsive blastoid natural killer cell lymphomaC P Bower, G R Standen, J Pawade, et al.
Blood|November 5, 1997
Identification of T-cell epitopes on the Rhesus polypeptides in autoimmune hemolytic anemiaR N Barker, A M Hall, G R Standen, et al.
Lancet (London, England)|September 8, 1990
Rapid neonatal diagnosis of von Willebrand's disease by use of the polymerase chain reactionP Bignell, G R Standen, D J Bowen, et al.
Thrombosis and Haemostasis|January 1, 1997
Genetic diagnosis of factor V Leiden using heteroduplex technologyD J Bowen, G R Standen, S Granville, et al.
American Journal of Hematology|August 1, 1989
Myelodysplastic syndrome with trisomy 8 in an adolescent with Fanconi anaemia and selective IgA deficiencyG R Standen, I A Hughes, A D Geddes, et al.
Pageof 5