Associated Papers
Prediction of hemophilia A severity using a small-input machine-learning framework.
Lopes TJS et al.
Npj Systems Biology and Applications, 2021
34035274 (PubMed )
Supplement: 41540_2021_183_MOESM3_ESM.xlsx › Predictions___Clinical_reports
Genetic causes of haemophilia in women and girls.
Miller CH et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2021
Compensated pathogenic variants in coagulation factors VIII and IX present complex mapping between molecular impact and hemophilia severity.
Marín Ò et al.
Scientific Reports, 2019
31267011 (PubMed )
Supplement: 41598_2019_45916_MOESM2_ESM.xlsx › Variants_used
Identification of deep intronic individual variants in patients with hemophilia A by next-generation sequencing of the whole factor VIII gene.
Inaba H et al.
Research and Practice in Thrombosis and Haemostasis, 2017
Detection of factor VIII gene mutations by high-resolution melting analysis.
Laurie AD et al.
Clinical Chemistry, 2007
Effects of 7 hemoglobin variants on the measurement of glycohemoglobin by 14 analytical methods.
Lee ST et al.
Clinical Chemistry, 2007
The molecular aetiology of haemophilia A in a New Zealand patient group.
Laurie AD et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2007
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