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Additive color synthesis
Additive colour synthesis
Additive synthesis
Combustion synthesis
Metabolite synthesis
Reaction synthesis
Rule-based speech synthesis
Rule-based synthesis
SHS
Self-propagating high temperature synthesis
Self-propagating high-temperature synthesis
Subtractive color mixing
Subtractive color synthesis
Subtractive colour mixing
Subtractive colour synthesis
Subtractive synthesis
Summary report
Synthesis
Synthesis report
Synthesis-by-rule

Traduction de «metabolite synthesis » (Anglais → Français) :



self-propagating high-temperature synthesis [ SHS | self-propagating high temperature synthesis | combustion synthesis | reaction synthesis ]

synthèse autopropagée à haute température [ S.H.S. | synthèse auto-propagée à haute température | synthèse par réaction auto-entretenue à haute température | synthèse SHS ]


A heterogeneous group disorders characterized by short, brittle hair with low-sulfur content (due to an abnormal synthesis of the sulfur containing keratins). The abnormalities are usually obvious at birth, with variable clinical expression. Trichoth

trichothiodystrophie


rule-based synthesis [ rule-based speech synthesis | synthesis-by-rule ]

synthèse par règles [ synthèse à base de règles ]


additive colour synthesis [ additive color synthesis | additive synthesis ]

synthèse additive des couleurs [ synthèse additive ]


subtractive colour synthesis | subtractive color synthesis | subtractive synthesis | subtractive colour mixing | subtractive color mixing

synthèse soustractive | synthèse soustractive des couleurs | mélange soustractif | système soustractif


summary report | synthesis | synthesis report

rapport de synthèse | synthèse


additive colour synthesis | additive synthesis

synthèse additive | synthèse des couleurs additive


A rare genetic disorder of metabolite absorption or transport with characteristics of persistently decreased riboflavin serum levels due to a primary genetic defect in the mother and which leads to clinical and biochemical findings consistent with a

déficit maternel en riboflavine


A mitochondrial disease due to a defect in mitochondrial protein synthesis resulting in deficiency of respiratory chain complexes I, III and IV in the cardiac and skeletal muscle and brain. The disease has characteristics of severe hypertrophic cardi

déficit combiné de la phosphorylation oxydative type 8


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