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A J Montandon

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Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 1, 1991
Genetics and molecular biology of haemophilias A and BP M Green, A J Montandon, D R Bentley, et al.
Nucleic Acids Research|August 11, 1989
Detection of novel genetic markers by mismatch analysisR G Roberts, A J Montandon, M Bobrow, et al.
Nucleic Acids Research|May 11, 1989
Direct detection of point mutations by mismatch analysis: application to haemophilia BA J Montandon, P M Green, F Giannelli, et al.
Thrombosis and Haemostasis|January 23, 1992
Haplotype analysis of identical factor IX mutants using PCRP M Green, A J Montandon, R Ljung, et al.
Lancet (London, England)|March 16, 1991
Detection of three novel mutations in two haemophilia A patients by rapid screening of whole essential region of factor VIII geneJ A Naylor, P M Green, A J Montandon, et al.
Nucleic Acids Research|June 11, 1990
The incidence and distribution of CpG----TpG transitions in the coagulation factor IX gene. A fresh look at CpG mutational hotspotsP M Green, A J Montandon, D R Bentley, et al.
Human Genetics|July 1, 1990
Two factor IX mutations in the family of an isolated haemophilia B patient: direct carrier diagnosis by amplification mismatch detection (AMD)A J Montandon, P M Green, D R Bentley, et al.
British Journal of Haematology|July 1, 1991
Haemophilia B mutations in a complete Swedish population sample: a test of new strategy for the genetic counselling of diseases with high mutational heterogeneityP M Green, A J Montandon, R Ljung, et al.
Human Genetics|May 1, 1992
Direct estimate of the haemophilia B (factor IX deficiency) mutation rate and of the ratio of the sex-specific mutation rates in SwedenA J Montandon, P M Green, D R Bentley, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 1, 1991
Genetics and molecular biology of haemophilias A and BP M Green, A J Montandon, D R Bentley, et al.
Nucleic Acids Research|August 11, 1989
Detection of novel genetic markers by mismatch analysisR G Roberts, A J Montandon, M Bobrow, et al.
Nucleic Acids Research|May 11, 1989
Direct detection of point mutations by mismatch analysis: application to haemophilia BA J Montandon, P M Green, F Giannelli, et al.
Thrombosis and Haemostasis|January 23, 1992
Haplotype analysis of identical factor IX mutants using PCRP M Green, A J Montandon, R Ljung, et al.
Lancet (London, England)|March 16, 1991
Detection of three novel mutations in two haemophilia A patients by rapid screening of whole essential region of factor VIII geneJ A Naylor, P M Green, A J Montandon, et al.
Nucleic Acids Research|June 11, 1990
The incidence and distribution of CpG----TpG transitions in the coagulation factor IX gene. A fresh look at CpG mutational hotspotsP M Green, A J Montandon, D R Bentley, et al.
Human Genetics|July 1, 1990
Two factor IX mutations in the family of an isolated haemophilia B patient: direct carrier diagnosis by amplification mismatch detection (AMD)A J Montandon, P M Green, D R Bentley, et al.
British Journal of Haematology|July 1, 1991
Haemophilia B mutations in a complete Swedish population sample: a test of new strategy for the genetic counselling of diseases with high mutational heterogeneityP M Green, A J Montandon, R Ljung, et al.
Human Genetics|May 1, 1992
Direct estimate of the haemophilia B (factor IX deficiency) mutation rate and of the ratio of the sex-specific mutation rates in SwedenA J Montandon, P M Green, D R Bentley, et al.
Pageof 1