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A C Goodeve

Showing results (21-30 of 43) with videos related to

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Thrombosis and Haemostasis|September 24, 1999
A common splice site mutation is shared by two families with different type 2N von Willebrand disease mutationsI M Nesbitt, K K Hampton, F E Preston, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 4, 2008
Re-evaluation of three Israeli families initially diagnosed with type 1 von Willebrand disease in light of the ISTH update on von Willebrand factor pathophysiology and classificationS M B Hashemi Soteh, J Anson, A Inbal, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|February 1, 1994
A comparison of the allelic frequencies of ten DNA polymorphisms associated with factor VIII and factor IX genes in Thai and Western European populationsA C Goodeve, A Chuansumrit, W Sasanakul, et al.
British Journal of Haematology|April 2, 2005
Aberrant methylation of the negative regulators RASSFIA, SHP-1 and SOCS-1 in myelodysplastic syndromes and acute myeloid leukaemiaM F Johan, D T Bowen, M E Frew, et al.
British Journal of Haematology|September 15, 2005
JAK2 V617F Mutation is uncommon in chronic myelomonocytic leukaemiaM F Johan, A C Goodeve, D T Bowen, et al.
Journal of Medical Screening|July 14, 2007
Is routine molecular screening for common alpha-thalassaemia deletions necessary as part of an antenatal screening programme?Y Sorour, S Heppinstall, N Porter, et al.
Thrombosis and Haemostasis|June 1, 1996
Characterisation of type 2N von Willebrand disease using phenotypic and molecular techniquesI M Nesbitt, A C Goodeve, A M Guilliatt, et al.
Leukemia|July 28, 2007
Gene structure, expression profiling and mutation analysis of the tumour suppressor SHIP1 in Caucasian acute myeloid leukaemiaD C Gilby, A C Goodeve, P R Winship, et al.
British Journal of Haematology|April 7, 1999
A rapid method for haemophilia B mutation detection using conformation sensitive gel electrophoresisJ L Hinks, P R Winship, M Makris, et al.
Journal of Medical Virology|May 1, 1992
Detection of EBV DNA in post-nasal space biopsy tissue from asymptomatic EBV-seropositive individualsJ F Lees, A C Goodeve, J E Arrand, et al.
Pageof 5

Showing results (21-30 of 43) with videos related to

Sort By:
Pageof 5
Thrombosis and Haemostasis|September 24, 1999
A common splice site mutation is shared by two families with different type 2N von Willebrand disease mutationsI M Nesbitt, K K Hampton, F E Preston, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 4, 2008
Re-evaluation of three Israeli families initially diagnosed with type 1 von Willebrand disease in light of the ISTH update on von Willebrand factor pathophysiology and classificationS M B Hashemi Soteh, J Anson, A Inbal, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|February 1, 1994
A comparison of the allelic frequencies of ten DNA polymorphisms associated with factor VIII and factor IX genes in Thai and Western European populationsA C Goodeve, A Chuansumrit, W Sasanakul, et al.
British Journal of Haematology|April 2, 2005
Aberrant methylation of the negative regulators RASSFIA, SHP-1 and SOCS-1 in myelodysplastic syndromes and acute myeloid leukaemiaM F Johan, D T Bowen, M E Frew, et al.
British Journal of Haematology|September 15, 2005
JAK2 V617F Mutation is uncommon in chronic myelomonocytic leukaemiaM F Johan, A C Goodeve, D T Bowen, et al.
Journal of Medical Screening|July 14, 2007
Is routine molecular screening for common alpha-thalassaemia deletions necessary as part of an antenatal screening programme?Y Sorour, S Heppinstall, N Porter, et al.
Thrombosis and Haemostasis|June 1, 1996
Characterisation of type 2N von Willebrand disease using phenotypic and molecular techniquesI M Nesbitt, A C Goodeve, A M Guilliatt, et al.
Leukemia|July 28, 2007
Gene structure, expression profiling and mutation analysis of the tumour suppressor SHIP1 in Caucasian acute myeloid leukaemiaD C Gilby, A C Goodeve, P R Winship, et al.
British Journal of Haematology|April 7, 1999
A rapid method for haemophilia B mutation detection using conformation sensitive gel electrophoresisJ L Hinks, P R Winship, M Makris, et al.
Journal of Medical Virology|May 1, 1992
Detection of EBV DNA in post-nasal space biopsy tissue from asymptomatic EBV-seropositive individualsJ F Lees, A C Goodeve, J E Arrand, et al.
Pageof 5