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I R Peake

Showing results (81-90 of 120) with videos related to

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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.
British Journal of Haematology|January 1, 1995
Rapid genotype analysis in type 2B von Willebrand's disease using a universal heteroduplex generatorN Wood, G R Standen, E W Murray, 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.
British Journal of Haematology|September 1, 1983
The interaction between factor VIII clotting antigen (VIIICAg) and phospholipidA Yoshioka, I R Peake, B L Furlong, et al.
Clinical and Laboratory Haematology|January 1, 1992
The relationship of HIV-1 viral sequences detected by the polymerase chain reaction in haemophilic patients to clinical and other markers of infectionA H Dannatt, S J Goodwin, H Dasani, et al.
Blood|September 1, 1996
Molecular basis of protein S deficiency in three families also showing independent inheritance of factor V leidenN J Beauchamp, M E Daly, P C Cooper, et al.
British Journal of Haematology|August 1, 1981
Carrier detection in haemophilia a by immunological measurement of factor VIII related antigen (VIIIRAg) and factor VIII clotting antigen (VIIICAg)I R Peake, R G Newcombe, B L Davies, et al.
Blood|August 1, 1990
Family studies and prenatal diagnosis in severe von Willebrand disease by polymerase chain reaction amplification of a variable number tandem repeat region of the von Willebrand factor geneI R Peake, D Bowen, P Bignell, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health|January 1, 1995
DNA polymorphisms for carrier detection of hemophilia in ThailandA Chuansumrit, A Goodeve, W Sasanakul, et al.
British Journal of Haematology|August 1, 1989
Factor IX Cardiff: a variant factor IX protein that shows abnormal activation is caused by an arginine to cysteine substitution at position 145M B Liddell, I R Peake, S A Taylor, et al.
Pageof 12

Showing results (81-90 of 120) with videos related to

Sort By:
Pageof 12
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.
British Journal of Haematology|January 1, 1995
Rapid genotype analysis in type 2B von Willebrand's disease using a universal heteroduplex generatorN Wood, G R Standen, E W Murray, 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.
British Journal of Haematology|September 1, 1983
The interaction between factor VIII clotting antigen (VIIICAg) and phospholipidA Yoshioka, I R Peake, B L Furlong, et al.
Clinical and Laboratory Haematology|January 1, 1992
The relationship of HIV-1 viral sequences detected by the polymerase chain reaction in haemophilic patients to clinical and other markers of infectionA H Dannatt, S J Goodwin, H Dasani, et al.
Blood|September 1, 1996
Molecular basis of protein S deficiency in three families also showing independent inheritance of factor V leidenN J Beauchamp, M E Daly, P C Cooper, et al.
British Journal of Haematology|August 1, 1981
Carrier detection in haemophilia a by immunological measurement of factor VIII related antigen (VIIIRAg) and factor VIII clotting antigen (VIIICAg)I R Peake, R G Newcombe, B L Davies, et al.
Blood|August 1, 1990
Family studies and prenatal diagnosis in severe von Willebrand disease by polymerase chain reaction amplification of a variable number tandem repeat region of the von Willebrand factor geneI R Peake, D Bowen, P Bignell, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health|January 1, 1995
DNA polymorphisms for carrier detection of hemophilia in ThailandA Chuansumrit, A Goodeve, W Sasanakul, et al.
British Journal of Haematology|August 1, 1989
Factor IX Cardiff: a variant factor IX protein that shows abnormal activation is caused by an arginine to cysteine substitution at position 145M B Liddell, I R Peake, S A Taylor, et al.
Pageof 12