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Accelerator factor
Audiogram Fletcher and Wegel
Autoprothrombin C
Coagulation factor X
FX
Factor V
Factor X
Fletcher Challenge Canada Limited
Fletcher factor
Fletcher factor deficiency
Fletcher trait
Fletcher's factor
Labile factor
Owren factor
Plasma accelerator globulin
Plasma labile factor
Plasma prothrombins conversion factor
Pre-kallikrein deficiency
Prekallikrein
Prekallikrein deficiency
Proaccelerin
Prothrombin accelerator
Prower factor
Stuart factor
Stuart-Prower factor

Translation of "Fletcher factor " (English → French) :

prekallikrein | Fletcher factor | Fletcher's factor

prékallikréine | facteur Fletcher


fletcher trait | prekallikrein deficiency | pre-kallikrein deficiency | Fletcher factor deficiency

déficit en prékallicréine | déficit en facteur Fletcher


factor V | proaccelerin | accelerator factor | Owren factor | labile factor | plasma accelerator globulin | plasma labile factor | plasma prothrombins conversion factor | prothrombin accelerator

facteur V | proaccélérine | accélérine | facteur labile | facteur accélérateur | facteur d'Owren


Stuart factor [ Stuart-Prower factor | factor X | FX | coagulation factor X | autoprothrombin C | Prower factor ]

facteur Stuart [ facteur X ]


Belle Eau Claire Investments Ltd. and George Alexander Fletcher Remission Order

Décret de remise visant Belle Eau Claire Investments Ltd. et George Alexander Fletcher


Fletcher Challenge Canada Limited

Fletcher Challenge Canada Limitée


Short stature due to primary acid-labile subunit (ALS) deficiency is characterized by moderate postnatal growth deficit, markedly low circulating levels of insulin-like growth factor 1 (IGF-1) and insulin-like growth factor binding protein 3 (IGFBP-3

petite taille par déficit primaire en sous-unité acide labile




Syndrome that is characterized by the association of multiple sclerosis with lamellar ichthyosis and hematological anomalies (beta thalassemia minor and a quantitative deficit of factor VIII-von Willebrand complex). Other clinical manifestations may

syndrome de sclérose en plaques-ichtyose-déficit en facteur VIII


An inherited bleeding disorder caused by the reduction in activity and antigen levels of both factor V and factor VIII with manifestation of mild-to-moderate bleeding symptoms. Caused by mutations either in the LMAN1 gene (chromosome 18; q21) or in t

déficit combiné en facteurs V et VIII




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'Fletcher factor' ->

Date index: 2021-07-11
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