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Accelerator factor
Antibiotic resistance plasmid
Autoprothrombin C
Coagulation factor X
Drug-resistance factor
FX
Factor V
Factor X
HX
Humidex
Humidex and its Use in the Workplace
Humidex factor
Humidex index
Humidex indicator
Labile factor
Owren factor
Plasma accelerator globulin
Plasma labile factor
Plasma prothrombins conversion factor
Proaccelerin
Prothrombin accelerator
Prower factor
R-factor
R-factor plasmid
R-plasmid
RPA factor
RPB factor
Remaining principal amount factor
Remaining principal balance factor
Resistance factor
Resistance plasmid
Stuart factor
Stuart-Prower factor

Traduction de «Humidex factor » (Anglais → Français) :

humidex | HX | humidex index | humidex factor | humidex indicator

humidex | indice humidex | IH | facteur humidex


Humidex and its Use in the Workplace

L'indice d'humidité et ses applications sur les lieux de travail




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 ]


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


remaining principal amount factor | RPA factor | RPB factor | remaining principal balance factor

indice du principal restant


antibiotic resistance plasmid | drug-resistance factor | resistance factor | resistance plasmid | R-factor | R-factor plasmid | R-plasmid

facteur de résistance | facteur de transfert de résistance | facteur R | plasmide de résistance


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


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




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'Humidex factor' ->

Date index: 2022-09-19
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