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P H Reitsma

Showing results (81-90 of 275) with videos related to

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Nucleic Acids Research|October 25, 1989
MspI RFLP in intron 8 of the human protein C geneE Koenhen, R M Bertina, P H Reitsma
Journal of Thrombosis and Haemostasis : JTH|October 26, 2018
More kudosF R Rosendaal, F Johnstone, P H Reitsma
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 24, 2016
The inheritance and molecular genetics of von Willebrand's diseaseJ C Eikenboom, P H Reitsma, E Briët
Human Genetics|August 1, 1995
The mutational demography of protein C deficiencyM Krawczak, P H Reitsma, D N Cooper
Thrombosis and Haemostasis|May 3, 1993
Double strand conformation polymorphism (DSCP) detects two point mutations at codon 280 (AAC-->ATC) and at codon 431 (TAC-->AAC) of the blood coagulation factor VIII geneW C Pieneman, P H Reitsma, E Briët
Journal of Thrombosis and Haemostasis : JTH|September 14, 2011
Not exclusively tissue factor: neutrophil extracellular traps provide another link between chemotherapy and thrombosisY W Van Den Berg, P H Reitsma
Annals of Hematology|March 1, 1994
Seeming homozygosity in type-IIB von Willebrand's disease due to a polymorphism within the sequence of a commonly used primerJ C Eikenboom, P H Reitsma, E Briët
Human Molecular Genetics|October 1, 1993
Amino acid dimorphism in IL1A is detectable by PCR amplificationP A van den Velden, P H Reitsma
Thrombosis and Haemostasis|June 1, 1996
Inherited prethrombotic disorders and infectious purpuraR G Westendorp, P H Reitsma, R M Bertina
FEBS Letters|September 17, 1990
Localization of transcription initiation sites in the human coagulation factor IX geneM J Reijnen, R M Bertina, P H Reitsma
Pageof 28

Showing results (81-90 of 275) with videos related to

Sort By:
Pageof 28
Nucleic Acids Research|October 25, 1989
MspI RFLP in intron 8 of the human protein C geneE Koenhen, R M Bertina, P H Reitsma
Journal of Thrombosis and Haemostasis : JTH|October 26, 2018
More kudosF R Rosendaal, F Johnstone, P H Reitsma
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 24, 2016
The inheritance and molecular genetics of von Willebrand's diseaseJ C Eikenboom, P H Reitsma, E Briët
Human Genetics|August 1, 1995
The mutational demography of protein C deficiencyM Krawczak, P H Reitsma, D N Cooper
Thrombosis and Haemostasis|May 3, 1993
Double strand conformation polymorphism (DSCP) detects two point mutations at codon 280 (AAC-->ATC) and at codon 431 (TAC-->AAC) of the blood coagulation factor VIII geneW C Pieneman, P H Reitsma, E Briët
Journal of Thrombosis and Haemostasis : JTH|September 14, 2011
Not exclusively tissue factor: neutrophil extracellular traps provide another link between chemotherapy and thrombosisY W Van Den Berg, P H Reitsma
Annals of Hematology|March 1, 1994
Seeming homozygosity in type-IIB von Willebrand's disease due to a polymorphism within the sequence of a commonly used primerJ C Eikenboom, P H Reitsma, E Briët
Human Molecular Genetics|October 1, 1993
Amino acid dimorphism in IL1A is detectable by PCR amplificationP A van den Velden, P H Reitsma
Thrombosis and Haemostasis|June 1, 1996
Inherited prethrombotic disorders and infectious purpuraR G Westendorp, P H Reitsma, R M Bertina
FEBS Letters|September 17, 1990
Localization of transcription initiation sites in the human coagulation factor IX geneM J Reijnen, R M Bertina, P H Reitsma
Pageof 28