A. I. Wacey

Molecular analysis of the genotype-phenotype relationship in factor X deficiency

David Millar, Linda Elliston, P. Deex et al. · Human Genetics · 2000 · 127 citations

Factor X Deficiency, Genetic Disorder, Genetics +8

Molecular defects in CRM+ factor VII deficiencies: modelling of missense mutations in the catalytic domain of FVII

Francesco Bernardi, David Liney, P. Patracchini et al. · British Journal of Haematology · 1994 · 56 citations

The haemophilia A mutation search test and resource site, home page of the factor VIII mutation database: HAMSTeRS

A. I. Wacey · Nucleic Acids Research · 1996 · 31 citations · Full text

A molecular model of the serine protease domain of activated protein C: application to the study of missense mutations causing protein C deficiency

A. I. Wacey, Susan Pemberton, D.N. Cooper et al. · British Journal of Haematology · 1993 · 26 citations

Serine Protease Domain, Protein Assembly, Molecular Biology +16

Three novel missense mutations in the antithrombin III (AT3) gene causing recurrent venous thrombosis

DavidS. Millar, A. I. Wacey, Jennifer Ribando et al. · Human Genetics · 1994 · 23 citations

Thrombosis, Venous Disease, Venous Thrombosis +12