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Antibiotic resistance plasmid
Appraise risk factors
Assess risk factors
Check risk factors
Drug-resistance factor
Fish anatomy
Forms of fish anatomy
Geomorphology
Lexicological factoring
Morphological factoring
Morphology
Morphology of the earth
R-factor
R-factor plasmid
R-plasmid
Range of fish morphology
Resistance factor
Resistance plasmid
Risk factor assessment
Scope of fish morphology
Soil morphology

Vertaling van "Morphological factoring " (Engels → Nederlands) :

lexicological factoring | morphological factoring

lexicologische analyse | morfologische analyse


range of fish morphology | scope of fish morphology | fish anatomy | forms of fish anatomy

anatomie van vissen




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

kleine gestalte door primaire zuurlabiele subeenheiddeficiëntie


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

resistentie-factor | R-factor


appraise risk factors | check risk factors | assess risk factors | risk factor assessment

risicofactoren beoordelen | risicofactoren inschatten


classify the factors causing changes in food during storage | establish the factors causing changes in food during storage | analyse the factors causing changes in food during storage | identify the factors causing changes in food during storage

factoren identificeren die veranderingen tijdens de opslag van voedingsmiddelen veroorzaken


geomorphology [ morphology of the earth ]

geomorfologie


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

multiple sclerose, ichthyosis, factor VIII-deficiëntiesyndroom


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

gecombineerde deficiëntie van factor V en factor VIII




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Date index: 2023-08-02
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