Development of resistance to activated protein C during pregnancy

A. M. Cumming, Robert C. Tait, S. Fildes, +3

British Journal of Haematology

Weeks GestationGynecologyEmbryologyHigh-risk PregnancyMaternal Immunization +17

HLA Class II Profile: A Weak Determinant of Factor VIII Inhibitor Development in Severe Haemophilia A

C. R. M. Hay, W. E. R. Oilier, L Pepper, +7

Thrombosis and Haemostasis

The prothrombin gene G20210A variant: prevalence in a U.K. anticoagulant clinic population

A. M. Cumming, S. Keeney, A. Salden, +3

British Journal of Haematology

GeneticsGenetic EpidemiologyHuman PolymorphismPathologyProthrombin Gene +19

An investigation of the von Willebrand factor genotype in UK patients diagnosed to have type 1 von Willebrand disease

P. M. Grundy, S. Keeney, Will Lester, +10

Thrombosis and Haemostasis

A common ancestral mutation (C128X) occurring in 11 non‐Jewish families from the UK with factor XI deficiency

Paula Bolton‐Maggs, Hava Peretz, Rachel Butler, +5

Journal of Thrombosis and Haemostasis

Mendelian DisorderNon‐jewish FamiliesGenetic DisorderGeneticsGenetic Epidemiology +5

The molecular analysis of haemophilia A: a guideline from the UK haemophilia centre doctors’ organization haemophilia genetics laboratory network

S. Keeney, Michael Mitchell, Anne Goodeve

Haemophilia

The molecular analysis of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors’ Organisation Haemophilia Genetics Laboratory Network

S. Keeney, D. Bowen, A. M. Cumming, +3

Haemophilia

A novel deletion mutation is recurrent in von Willebrand disease types 1 and 3

M. S. Sutherland, A. M. Cumming, Mackenzie Bowman, +6

Blood

The mutation spectrum associated with type 3 von Willebrand disease in a cohort of patients from the North West of England

M. S. Sutherland, S. Keeney, Paula Bolton‐Maggs, +3

Haemophilia

GeneticsGenetic EpidemiologyPathologyMolecular GeneticsSingle Vwf Mutation +18

Type 2N von Willebrand disease: rapid genetic diagnosis of G2811A (R854Q), C2696T (R816W), T2701A (H817Q) and G2823T (C858F)--detection of a novel candidate type 2N mutation: C2810T (R854W).

D. J. Bowen, Graham R. Standen, Claudine Mazurier, +4

PubMed

GeneticsGenetic EpidemiologyPathologyMolecular BiologyMolecular Genetics +14