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Bacterial DNA
Bacterial desoxyribonucleic acid
Chromosomal DNA
Chromosomal desoxyribonucleic acid
DNA
Desoxiribo-suclein-acid
Desoxyribonucleic acid
Mitochondrial DNA
Mitochondrial RNA
Mitochondrial desoxyribonucleic acid
Mitochondrial ribonucleic acid

Translation of "Mitochondrial desoxyribonucleic acid " (English → French) :

mitochondrial desoxyribonucleic acid | mitochondrial DNA

acide désoxyribonucléique mitochondrial | ADN mitochondrial | ADN mit [Abbr.]
IATE - Health | Natural and applied sciences
IATE - Health | Natural and applied sciences


desoxiribo-suclein-acid | desoxyribonucleic acid [ DNA ]

acide désoxyribonucléique | acide désoxyribo nucléique [ ADN ]
Medicine & biology
Biologie (Sciences médicales et biologiques) | Biochimie - biophysique (Sciences médicales et biologiques)


mitochondrial ribonucleic acid | mitochondrial RNA

acide ribonucléique mitochondrial | ARN mitochondrial
biologie > biochimie
biologie > biochimie


desoxyribonucleic acid | DNA

acide désoxyribonucléique | ADN
biologie > biologie moléculaire | biologie > génétique
biologie > biologie moléculaire | biologie > génétique


Desoxyribonucleic acid | DNA

acide désoxyribonucléique | ADN
génie génétique | génétique moléculaire
génie génétique > génétique moléculaire


bacterial desoxyribonucleic acid | bacterial DNA

acide désoxyribonucléique bactérien | ADN bactérien
IATE - Health
IATE - Health


chromosomal desoxyribonucleic acid | chromosomal DNA

acide désoxyribonucléique extrachromosomique | ADN extrachromosomique
IATE - Health
IATE - Health


A mitochondrial fatty acid oxidation disorder characterized by hyperinsulinemic hypoglycemia with seizures, and in one case fulminant hepatic failure. Less than 10 cases have been reported to date. The disease can present in infancy or early childhoo

hyperinsulinisme par déficit en 3-hydroxylacyl-CoA déshydrogénase des acides gras à chaîne courte
SNOMEDCT-BE (disorder) / 721236002
SNOMEDCT-BE (disorder) / 721236002


A rare mitochondrial oxidative phosphorylation disorder due to nuclear deoxyribonucleic acid anomalies. The disease is characterised by progressive external ophthalmoplegia without diplopia, cerebellar atrophy, proximal skeletal muscle weakness with

syndrome d'OEP-myopathie-émaciation
SNOMEDCT-BE (disorder) / 764733009
SNOMEDCT-BE (disorder) / 764733009


A rare mitochondrial oxidative phosphorylation disorder due to nuclear deoxyribonucleic acid anomalies. The disease is characterized by progressive external ophthalmoplegia without diplopia, cerebellar atrophy, proximal skeletal muscle weakness with

syndrome d'ophtalmoplégie externe progressive-myopathie-émaciation
SNOMEDCT-BE (disorder) / 764733009
SNOMEDCT-BE (disorder) / 764733009




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'Mitochondrial desoxyribonucleic acid'

Date index:2021-04-09 -

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