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

Gillian Mellars

Showing results (1-10 of 5) with videos related to

Pageof 1
Sort By:
Methods in Molecular Biology (Clifton, N.J.)|October 13, 2010
Mutation detection by Southern blottingGillian Mellars, Keith Gomez
Thrombosis and Haemostasis|August 5, 2009
Structural analysis of eight novel and 112 previously reported missense mutations in the interactive FXI mutation database reveals new insight on FXI deficiencyRebecca E Saunders, Nuha Shiltagh, Keith Gomez, et al.
Thrombosis and Haemostasis|November 8, 2005
Detection of known haemophilia B mutations and carrier testing by microarrayKaimin Chan, W Sasanakul, Gillian Mellars, et al.
Blood|August 19, 2009
Characterization of W1745C and S1783A: 2 novel mutations causing defective collagen binding in the A3 domain of von Willebrand factorAnne F Riddell, Keith Gomez, Carolyn M Millar, et al.
Blood|January 26, 2011
Noninvasive prenatal diagnosis of hemophilia by microfluidics digital PCR analysis of maternal plasma DNANancy B Y Tsui, Rezan A Kadir, K C Allen Chan, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Methods in Molecular Biology (Clifton, N.J.)|October 13, 2010
Mutation detection by Southern blottingGillian Mellars, Keith Gomez
Thrombosis and Haemostasis|August 5, 2009
Structural analysis of eight novel and 112 previously reported missense mutations in the interactive FXI mutation database reveals new insight on FXI deficiencyRebecca E Saunders, Nuha Shiltagh, Keith Gomez, et al.
Thrombosis and Haemostasis|November 8, 2005
Detection of known haemophilia B mutations and carrier testing by microarrayKaimin Chan, W Sasanakul, Gillian Mellars, et al.
Blood|August 19, 2009
Characterization of W1745C and S1783A: 2 novel mutations causing defective collagen binding in the A3 domain of von Willebrand factorAnne F Riddell, Keith Gomez, Carolyn M Millar, et al.
Blood|January 26, 2011
Noninvasive prenatal diagnosis of hemophilia by microfluidics digital PCR analysis of maternal plasma DNANancy B Y Tsui, Rezan A Kadir, K C Allen Chan, et al.
Pageof 1