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A Goodeve

Showing results (11-20 of 37) with videos related to

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Blood|April 15, 1997
BCR-ABL transcript with an e19a2 (c3a2) junction in classical chronic myeloid leukemiaG Wilson, L Frost, A Goodeve, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 22, 2008
The molecular analysis of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organisation Haemophilia Genetics Laboratory NetworkS Keeney, D Bowen, A Cumming, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 24, 2010
F8 and F9 mutations fail to co-segregate in a family with co-incident haemophilia A and BS Siddiq, C Morse, A Goodeve, et al.
The Journal of Hygiene|February 1, 1983
A graded-dose study of inactivated, surface antigen influenza B vaccine in volunteers: reactogenicity, antibody response and protection to challenge virus infectionA Goodeve, C W Potter, A Clark, et al.
Thrombosis and Haemostasis|November 2, 1999
Inversion of intron 22 of the factor VIII gene in a girl with severe hemophilia A and Turner's syndromeA Chuansumrit, W Sasanakul, A Goodeve, et al.
Journal of Thrombosis and Haemostasis : JTH|December 15, 2010
Effect of the VWF promoter (GT)n repeat and single-nucleotide polymorphism c.-2527G>A on circulating von Willebrand factor levels under normal conditionsN Hickson, D Hampshire, G Castaman, et al.
Haematologica|May 9, 2000
Experience of a single Italian center in genetic counseling for hemophilia: from linkage analysis to molecular diagnosisG Tagariello, D Belvini, R Salviato, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 26, 2014
Genetic testing in bleeding disordersC de Brasi, O El-Maarri, D J Perry, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 3, 2016
Confirmation of genetic testing results in haemostasis and thrombosis - survey of current practice in the fieldI Jennings, A Goodeve, B Theophilus, et al.
Human Mutation|September 30, 1999
A study of Wilson disease mutations in BritainD Curtis, M Durkie, P Balac (Morris), et al.
Pageof 4

Showing results (11-20 of 37) with videos related to

Sort By:
Pageof 4
Blood|April 15, 1997
BCR-ABL transcript with an e19a2 (c3a2) junction in classical chronic myeloid leukemiaG Wilson, L Frost, A Goodeve, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 22, 2008
The molecular analysis of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organisation Haemophilia Genetics Laboratory NetworkS Keeney, D Bowen, A Cumming, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 24, 2010
F8 and F9 mutations fail to co-segregate in a family with co-incident haemophilia A and BS Siddiq, C Morse, A Goodeve, et al.
The Journal of Hygiene|February 1, 1983
A graded-dose study of inactivated, surface antigen influenza B vaccine in volunteers: reactogenicity, antibody response and protection to challenge virus infectionA Goodeve, C W Potter, A Clark, et al.
Thrombosis and Haemostasis|November 2, 1999
Inversion of intron 22 of the factor VIII gene in a girl with severe hemophilia A and Turner's syndromeA Chuansumrit, W Sasanakul, A Goodeve, et al.
Journal of Thrombosis and Haemostasis : JTH|December 15, 2010
Effect of the VWF promoter (GT)n repeat and single-nucleotide polymorphism c.-2527G>A on circulating von Willebrand factor levels under normal conditionsN Hickson, D Hampshire, G Castaman, et al.
Haematologica|May 9, 2000
Experience of a single Italian center in genetic counseling for hemophilia: from linkage analysis to molecular diagnosisG Tagariello, D Belvini, R Salviato, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 26, 2014
Genetic testing in bleeding disordersC de Brasi, O El-Maarri, D J Perry, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 3, 2016
Confirmation of genetic testing results in haemostasis and thrombosis - survey of current practice in the fieldI Jennings, A Goodeve, B Theophilus, et al.
Human Mutation|September 30, 1999
A study of Wilson disease mutations in BritainD Curtis, M Durkie, P Balac (Morris), et al.
Pageof 4