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C B Grundy

Showing results (1-10 of 11) with videos related to

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Human Genetics|August 1, 1992
A novel homozygous missense mutation in the protein C (PROC) gene causing recurrent venous thrombosisC B Grundy, M Chisholm, V V Kakkar, et al.
Human Genetics|August 1, 1992
Two different missense mutations at Arg 178 of the protein C (PROC) gene causing recurrent venous thrombosisC B Grundy, S Schulman, L Tengborn, et al.
Human Genetics|March 1, 1992
Protein C deficiency and thromboembolism: recurrent mutation at Arg 306 in the protein C geneC B Grundy, S Schulman, M Krawczak, et al.
Human Genetics|January 1, 1991
Molecular genetic analysis of factor X deficiency: gene deletion and germline mosaicismK Wieland, D S Millar, C B Grundy, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|April 1, 1993
A Gla domain mutation (Arg 15-->Trp) in the protein C (PROC) gene causing type 2 protein C deficiency and recurrent venous thrombosisD S Millar, C B Grundy, P Bignell, et al.
Human Genetics|March 1, 1993
A novel nonsense mutation in the protein C (PROC) gene (Trp-29-->term) causing recurrent venous thrombosisD S Millar, C B Grundy, P Bignell, et al.
Blood|August 15, 1991
Recurrent deletion in the human antithrombin III geneC B Grundy, F Thomas, D S Millar, et al.
Human Genetics|August 1, 1990
Improved carrier detection of haemophilia A using novel RFLPs at the DXS115 (767) locusP Jedlicka, S Greer, D S Millar, et al.
Genomics|August 1, 1992
De novo splice site mutation in the antithrombin III (AT3) gene causing recurrent venous thrombosis: demonstration of exon skipping by ectopic transcript analysisL P Berg, C B Grundy, F Thomas, et al.
Human Genetics|December 1, 1990
The molecular genetic analysis of haemophilia A; characterization of six partial deletions in the factor VIII geneD S Millar, R A Steinbrecher, K Wieland, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Human Genetics|August 1, 1992
A novel homozygous missense mutation in the protein C (PROC) gene causing recurrent venous thrombosisC B Grundy, M Chisholm, V V Kakkar, et al.
Human Genetics|August 1, 1992
Two different missense mutations at Arg 178 of the protein C (PROC) gene causing recurrent venous thrombosisC B Grundy, S Schulman, L Tengborn, et al.
Human Genetics|March 1, 1992
Protein C deficiency and thromboembolism: recurrent mutation at Arg 306 in the protein C geneC B Grundy, S Schulman, M Krawczak, et al.
Human Genetics|January 1, 1991
Molecular genetic analysis of factor X deficiency: gene deletion and germline mosaicismK Wieland, D S Millar, C B Grundy, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|April 1, 1993
A Gla domain mutation (Arg 15-->Trp) in the protein C (PROC) gene causing type 2 protein C deficiency and recurrent venous thrombosisD S Millar, C B Grundy, P Bignell, et al.
Human Genetics|March 1, 1993
A novel nonsense mutation in the protein C (PROC) gene (Trp-29-->term) causing recurrent venous thrombosisD S Millar, C B Grundy, P Bignell, et al.
Blood|August 15, 1991
Recurrent deletion in the human antithrombin III geneC B Grundy, F Thomas, D S Millar, et al.
Human Genetics|August 1, 1990
Improved carrier detection of haemophilia A using novel RFLPs at the DXS115 (767) locusP Jedlicka, S Greer, D S Millar, et al.
Genomics|August 1, 1992
De novo splice site mutation in the antithrombin III (AT3) gene causing recurrent venous thrombosis: demonstration of exon skipping by ectopic transcript analysisL P Berg, C B Grundy, F Thomas, et al.
Human Genetics|December 1, 1990
The molecular genetic analysis of haemophilia A; characterization of six partial deletions in the factor VIII geneD S Millar, R A Steinbrecher, K Wieland, et al.
Pageof 2