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Biochemical engineer
Biochemical engineering consultant
Biochemical manufacturing training materials writing
Biochemical procedures of cider production
Biochemical process
Biochemical process of cider production
Biochemical processes
Biochemical processes of cider production
Biochemical research engineer
Biochemical routes
Biochemical substance
Biochemical substances
Biological processes
Develop biochemical manufacturing training materials
Enzyme engineer
The biochemical processes of cider production
Wet conversion routes
Write biochemical manufacturing training materials

Vertaling van "Biochemical routes " (Engels → Nederlands) :

biochemical routes | biological processes | wet conversion routes

biologische processen


biochemical procedures of cider production | biochemical process of cider production | biochemical processes of cider production | the biochemical processes of cider production

biochemische processen bij de productie van cider


biochemical manufacturing training materials writing | developing biochemical manufacturing training materials | develop biochemical manufacturing training materials | write biochemical manufacturing training materials

opleidingsmateriaal voor biochemische productie ontwerpen | opleidingsmateriaal voor biochemische productie ontwikkelen


biochemical engineering consultant | biochemical research engineer | biochemical engineer | enzyme engineer

biochemisch ingenieur | laboratoriumingenieur biochemie | biochemicus | ingenieur biochemie


biochemical process | biochemical processes

biochemische processen


biochemical substance | biochemical substances

biochemische stoffen


Abnormal biochemical finding on antenatal screening of mother

afwijkende biochemische-bevindingen bij prenatale screening van moeder


A form of neuroacanthocytosis with clinical characteristics of a Huntington's disease-like phenotype with an involuntary hyperkinetic movement disorder, psychiatric manifestations and cognitive alterations, and biochemically by absence of the Kx anti

McLeod-neuroacanthocytosesyndroom


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

maternale riboflavinedeficiëntie


Disease that is characterized clinically by neonatal hyperpigmentation, hypoglycemia, failure to thrive, and recurrent infections and biochemically by glucocorticoid deficiency without mineralocorticoid deficiency. The disease usually presents in inf

familiale glucocorticoïdedeficiëntie


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