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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.
British Journal of Haematology|September 1, 1994
High prevalence of a mutation in the factor V gene within the U.K. population: relationship to activated protein C resistance and familial thrombosisN J Beauchamp, M E Daly, K K Hampton, 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.
Studies in Health Technology and Informatics|July 1, 2022
Structural and Semantic Mapping of Application Programming InterfacesAshley R Peake, Omar Khan, Sarah N Lim Choi Keung, et al.
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.
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.
Blood|June 7, 2003
Analysis of intracellular storage and regulated secretion of 3 von Willebrand disease-causing variants of von Willebrand factorGrégoire Michaux, Lindsay J Hewlett, Sarah L Messenger, 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.
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