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A C Goodeve

Showing results (31-40 of 43) with videos related to

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British Journal of Haematology|July 10, 2001
Identification of novel FLT-3 Asp835 mutations in adult acute myeloid leukaemiaF M Abu-Duhier, A C Goodeve, G A Wilson, et al.
British Journal of Haematology|July 10, 2001
Genomic structure of human FLT3: implications for mutational analysisF M Abu-Duhier, A C Goodeve, G A Wilson, et al.
Thrombosis and Haemostasis|May 25, 2001
A standard nomenclature for von Willebrand factor gene mutations and polymorphisms. On behalf of the ISTH SSC Subcommittee on von Willebrand factorA C Goodeve, J C Eikenboom, D Ginsburg, et al.
Thrombosis and Haemostasis|May 6, 1998
Precise carrier diagnosis in families with haemophilia A: use of conformation sensitive gel electrophoresis for mutation screening and polymorphism analysisI J Williams, A Abuzenadah, P R Winship, et al.
British Journal of Haematology|February 13, 2001
Are aberrant BCR--ABL transcripts more common than previously thought?G A Wilson, E A Vandenberghe, R C Pollitt, et al.
British Journal of Haematology|March 11, 2004
Mutations in PTPN11 are uncommon in adult myelodysplastic syndromes and acute myeloid leukaemiaM F Johan, D T Bowen, M E Frew, et al.
Thrombosis and Haemostasis|November 2, 1999
Null alleles are not a common cause of type 1 von Willebrand disease in the British populationT C Coughlan, J L Blagg, M Abulola, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|June 26, 2012
Genetics of haemostasisA C Goodeve, D J Perry, T Cumming, et al.
Hemoglobin|September 26, 2001
A second case of Hb Renert [beta133(H11)Val --> Ala]G Wilson, P Forrest, S Heppinstall, et al.
Blood|July 11, 2000
A novel von Willebrand disease-causing mutation (Arg273Trp) in the von Willebrand factor propeptide that results in defective multimerization and secretionS Allen, A M Abuzenadah, J Hinks, et al.
Pageof 5

Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
British Journal of Haematology|July 10, 2001
Identification of novel FLT-3 Asp835 mutations in adult acute myeloid leukaemiaF M Abu-Duhier, A C Goodeve, G A Wilson, et al.
British Journal of Haematology|July 10, 2001
Genomic structure of human FLT3: implications for mutational analysisF M Abu-Duhier, A C Goodeve, G A Wilson, et al.
Thrombosis and Haemostasis|May 25, 2001
A standard nomenclature for von Willebrand factor gene mutations and polymorphisms. On behalf of the ISTH SSC Subcommittee on von Willebrand factorA C Goodeve, J C Eikenboom, D Ginsburg, et al.
Thrombosis and Haemostasis|May 6, 1998
Precise carrier diagnosis in families with haemophilia A: use of conformation sensitive gel electrophoresis for mutation screening and polymorphism analysisI J Williams, A Abuzenadah, P R Winship, et al.
British Journal of Haematology|February 13, 2001
Are aberrant BCR--ABL transcripts more common than previously thought?G A Wilson, E A Vandenberghe, R C Pollitt, et al.
British Journal of Haematology|March 11, 2004
Mutations in PTPN11 are uncommon in adult myelodysplastic syndromes and acute myeloid leukaemiaM F Johan, D T Bowen, M E Frew, et al.
Thrombosis and Haemostasis|November 2, 1999
Null alleles are not a common cause of type 1 von Willebrand disease in the British populationT C Coughlan, J L Blagg, M Abulola, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|June 26, 2012
Genetics of haemostasisA C Goodeve, D J Perry, T Cumming, et al.
Hemoglobin|September 26, 2001
A second case of Hb Renert [beta133(H11)Val --> Ala]G Wilson, P Forrest, S Heppinstall, et al.
Blood|July 11, 2000
A novel von Willebrand disease-causing mutation (Arg273Trp) in the von Willebrand factor propeptide that results in defective multimerization and secretionS Allen, A M Abuzenadah, J Hinks, et al.
Pageof 5