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Publications by Marguerite Neerman-Arbez

Mutational Epidemiology of Congenital Fibrinogen Disorders

Thrombosis and Haemostasis

English

Dysfibrinogenaemia Associated With a Novel Heterozygous Mutation in FGB (C.680delG) and a Mild Clinical History of Bleeding

Blood Coagulation and Fibrinolysis

English

The 11 Kb FGA Deletion Responsible for Congenital Afibrinogenaemia Is Mediated by a Short Direct Repeat in the Fibrinogen Gene Cluster

European Journal of Human Genetics

English

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