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Accelerator factor
Agreement Embodying a Convention on Governance
Antibiotic resistance plasmid
Antihemophilic factor
Antihemophilic factor A
Drug-resistance factor
Factor V
Factor VIII
Factor VIII C
Labile factor
Owren factor
Plasma accelerator globulin
Plasma labile factor
Plasma prothrombins conversion factor
Proaccelerin
Prothrombin accelerator
R-factor
R-factor plasmid
R-plasmid
RPA factor
RPB
RPB Construction Ltee
RPB factor
Real Property Branch
Real Property Services
Real Property Services Branch
Remaining principal amount factor
Remaining principal balance factor
Resistance factor
Resistance plasmid

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

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

indice du principal restant
commerce > immobilier
commerce > immobilier


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
médecine > hématologie et sérologie | médecine > transfusion
médecine > hématologie et sérologie | médecine > transfusion


Real Property Branch [ RPB | Real Property Services | Real Property Services Branch ]

Direction générale des biens immobiliers [ DGBI | Services immobiliers | Direction générale des services immobiliers ]
Federal Government Bodies and Committees (Canadian)
Organismes et comités fédéraux (Gouvernement canadien)


Agreement Embodying a Convention on Governance between the Forces for Democratic Change, consisting of FRODEBU, RPB, PP, PL and the Political Parties of the Opposition, composed of UPRONA, RADDES, Inkinzo, PSD, ANADDE, ABASA, PIT, PRP, and PARENA [ Agreement Embodying a Convention on Governance ]

Accord portant convention de gouvernement entre les forces de changement démocratique constituées du FRODEBU, RPB, PP, PL, et les partis politiques de l'opposition constitués par UPRONA, RADDES, Inkinzo, PSD, ANADDE, ABASA, PIT, PRP, et PARENA [ Accord portant Convention de gouvernement ]
Titles of Conventions, Treaties and Agreements (Documents) | Political Science (General)
Titres de conventions, de traités et d'accords (Documents) | Sciences politiques (Généralités)


RPB Construction Ltee

RPB Construction Ltee
Private-Sector Bodies and Committees | Construction
Organismes et comités du secteur privé | Construction


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
SNOMEDCT-BE (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 / 721074002
SNOMEDCT-BE (disorder) / 721074002


factor VIII:C | factor VIII | antihemophilic factor | antihemophilic factor A

facteur VIII : C | facteur VIII coagulant | facteur VIII | facteur antihémophilique A | facteur VIII : C Ag
médecine > hématologie et sérologie | médecine > transfusion
médecine > hématologie et sérologie | médecine > transfusion


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
IATE - Natural and applied sciences
IATE - Natural and applied sciences


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
SNOMEDCT-BE (chromosome 18; q21) or in t / 715559004
SNOMEDCT-BE (disorder) / 715559004


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
SNOMEDCT-BE (beta thalassemia minor and a quantitative deficit of factor VIII-von Willebrand complex). Other clinical manifestations may / 733028000
SNOMEDCT-BE (disorder) / 733028000




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'RPB factor'

Date index:2022-06-22 -

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