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CDNA
Complementary DNA
Complementary deoxyribonucleic acid
DNA
DNA agar
DNA joinase
DNA ligase
DNA sealase
DNAse agar
DNase agar
DNase test agar
Deoxyribonuclease agar
Deoxyribonucleic acid
Deoxyribonucleic acid agar
Deoxyribonucleic acid ligase
Ligase
Polydeoxyribonucleotide synthetase
Polynucleotide ligase
Polynucleotide synthetase
R-DNA
Recombinant DNA
Recombinant deoxyribonucleic acid
Recombinant-DNA

Vertaling van "Complementary deoxyribonucleic acid " (Engels → Frans) :

complementary DNA | cDNA | complementary deoxyribonucleic acid

ADN complémentaire | ADN-c | ADN c | ADN copie | ADN c | ADN-c


recombinant deoxyribonucleic acid | recombinant DNA | recombinant-DNA | r-DNA [Abbr.]

acide désoxyribonucléique recombinant | ADN recombinant


deoxyribonucleic acid | DNA [Abbr.]

acide désoxyribonucléique | ADN [Abbr.]


Recommendation (92) 1 of 10 February 1992 of the Council of Europe Committee of Ministers on the use of Analysis of Deoxyribonucleic Acid (DNA) within the framework of the criminal justice system

Recommandation nº R (92) 1 du 10 février 1992 du Comité des ministres du Conseil de l'Europe relative à l'utilisation des analyses de l'acide désoxyribonucléique (ADN) dans le cadre du système de justice pénale


DNA [ deoxyribonucleic acid ]

ADN [ acide désoxyribonucléique ]


DNA ligase | deoxyribonucleic acid ligase | DNA joinase | DNA sealase | polynucleotide synthetase | polydeoxyribonucleotide synthetase | polynucleotide ligase | ligase

ADN ligase | ADN-ligase | polynucléotide ligase | DNA ligase | ligase


DNA | deoxyribonucleic acid

ADN | acide désoxyribonucléique | DNA


deoxyribonucleic acid agar [ DNA agar | deoxyribonuclease agar | DNase test agar | DNAse agar | DNase agar ]

gélose à l'acide désoxyribonucléique [ gélose à l'ADN | gélose DNase ]


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


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




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Date index: 2022-06-26
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