Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

D S Millar

Showing results (1-10 of 38) with videos related to

Pageof 4
Sort By:
Human Genetics|October 6, 1998
Variation of site-specific methylation patterns in the factor VIII (F8C) gene in human sperm DNAD S Millar, M Krawczak, D N Cooper
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|April 1, 1994
Screening for inversions in the factor VIII (F8) gene causing severe haemophilia AD S Millar, V V Kakkar, D N Cooper
The Journal of Biological Chemistry|April 26, 2000
A distinct sequence (ATAAA)n separates methylated and unmethylated domains at the 5'-end of the GSTP1 CpG islandD S Millar, C L Paul, P L Molloy, et al.
British Medical Journal (Clinical Research Ed.)|March 2, 1985
Fetal haematology in rhesus isoimmunisationK H Nicolaides, C H Rodeck, D S Millar, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 1, 1994
A homozygous deletion/insertion mutation in the protein C (PROC) gene causing neonatal Purpura fulminans: prenatal diagnosis in an at-risk pregnancyD S Millar, J Allgrove, C Rodeck, et al.
Human Genetics|September 1, 1991
The molecular genetics of haemophilia A: screening for point mutations in the factor VIII gene using the restriction enzyme TaqID S Millar, B Zoll, U Martinowitz, et al.
Prenatal Diagnosis|November 1, 1992
Prenatal exclusion of haemophilia A and carrier testing by direct detection of a disease lesionM Schwartz, D N Cooper, D S Millar, et al.
Journal of Medical Genetics|July 1, 1995
Population differences in the frequency of the factor V Leiden variant among people with clinically symptomatic protein C deficiencyP J Hallam, D S Millar, M Krawczak, et al.
Human Genetics|May 1, 1991
Carrier detection in haemophilia A by direct analysis of factor VIII gene lesionsD S Millar, P J Green, B Zoll, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 1, 1993
A novel point mutation (Val 297-->Met) in the serine proteinase domain of protein C in a patient with both venous and arterial thromboembolic diseaseD S Millar, A I Wacey, J Voke, et al.
Pageof 4

Showing results (1-10 of 38) with videos related to

Sort By:
Pageof 4
Human Genetics|October 6, 1998
Variation of site-specific methylation patterns in the factor VIII (F8C) gene in human sperm DNAD S Millar, M Krawczak, D N Cooper
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|April 1, 1994
Screening for inversions in the factor VIII (F8) gene causing severe haemophilia AD S Millar, V V Kakkar, D N Cooper
The Journal of Biological Chemistry|April 26, 2000
A distinct sequence (ATAAA)n separates methylated and unmethylated domains at the 5'-end of the GSTP1 CpG islandD S Millar, C L Paul, P L Molloy, et al.
British Medical Journal (Clinical Research Ed.)|March 2, 1985
Fetal haematology in rhesus isoimmunisationK H Nicolaides, C H Rodeck, D S Millar, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 1, 1994
A homozygous deletion/insertion mutation in the protein C (PROC) gene causing neonatal Purpura fulminans: prenatal diagnosis in an at-risk pregnancyD S Millar, J Allgrove, C Rodeck, et al.
Human Genetics|September 1, 1991
The molecular genetics of haemophilia A: screening for point mutations in the factor VIII gene using the restriction enzyme TaqID S Millar, B Zoll, U Martinowitz, et al.
Prenatal Diagnosis|November 1, 1992
Prenatal exclusion of haemophilia A and carrier testing by direct detection of a disease lesionM Schwartz, D N Cooper, D S Millar, et al.
Journal of Medical Genetics|July 1, 1995
Population differences in the frequency of the factor V Leiden variant among people with clinically symptomatic protein C deficiencyP J Hallam, D S Millar, M Krawczak, et al.
Human Genetics|May 1, 1991
Carrier detection in haemophilia A by direct analysis of factor VIII gene lesionsD S Millar, P J Green, B Zoll, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 1, 1993
A novel point mutation (Val 297-->Met) in the serine proteinase domain of protein C in a patient with both venous and arterial thromboembolic diseaseD S Millar, A I Wacey, J Voke, et al.
Pageof 4