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Acquired mutation
DNM
De novo genetic mutation
De novo hearing
De novo mutation
Derivative
Frame shift mutation
Frameshift mutation
Gene mutation
Genetic mutation
Hearing de novo
Modified virus
Mutated virus
Mutation
New genetic mutation
Phase-shift mutation
Phaseshift mutation
Porto Novo
Porto-Novo
Reading frame shift
Reading-frame mutation
Rewrite of a virus
Rewritten version of a virus
Sign mutation
Somatic cell mutation
Somatic mutation

Translation of "de novo mutation " (English → French) :

de novo genetic mutation | de novo mutation | DNM | new genetic mutation

mutation génétique de novo | mutation de novo | nouvelle mutation génétique
biologie > génétique | médecine > sémiologie et pathologie
biologie > génétique | médecine > sémiologie et pathologie


frameshift mutation | frame shift mutation | phaseshift mutation | phase-shift mutation | reading-frame mutation | sign mutation | reading frame shift

mutation de changement de phase | mutation par décalage de code | mutation avec déphasage | mutation par déphasage | mutation à trame décalée | mutation par délation nucléotidique | mutation déterminant un décalage de lecture | mutation par insertion nucléotidique | mutation entraînant un changement de phase dans la lecture | mutation déplaçant le cadre de lecture | mutation par décalage du cadre de lecture du code génétique | décalage de trame | mutation frame-shift
biologie > génie génétique
biologie > génie génétique


Porto Novo [ Porto-Novo ]

Porto-Novo
Place Names (outside Canada)
Toponymes (hors Canada)


de novo hearing [ hearing de novo ]

audience de novo [ nouvelle audience ]
Rules of Court | Citizenship and Immigration
Règles de procédure | Citoyenneté et immigration


Ovarian cancer caused by germline mutations in various genes, usually associated with additional cancer risks. The most common are breast and ovarian cancer syndrome (HBOC) due to mutations in BRCA1 and BRCA2 genes and hereditary nonpolyposis colorec

syndrome héréditaire de prédisposition au cancer de l'ovaire
SNOMEDCT-BE (HBOC) due to mutations in BRCA1 and BRCA2 genes and hereditary nonpolyposis colorec / 771080008
SNOMEDCT-BE (disorder) / 771080008


acquired mutation | somatic cell mutation | somatic mutation

mutation somatique
IATE - Natural and applied sciences
IATE - Natural and applied sciences


mutation | gene mutation | genetic mutation

mutation | mutation génétique
biologie > génétique | biologie > génie génétique
biologie > génétique | biologie > génie génétique


A rare metabolic myopathy with characteristics of muscle cramping and/or stiffness after exercise (especially during heat exposure), post-exertional rhabdomyolysis and myoglobinuria and elevation of serum creatine kinase. Caused by mutation in the SL

myopathie métabolique par défaut de transport du lactate
SNOMEDCT-BE (especially during heat exposure), post-exertional rhabdomyolysis and myoglobinuria and elevation of serum creatine kinase. Caused by mutation in the SL / 766715000
SNOMEDCT-BE (disorder) / 766715000


mutated virus [ mutation | derivative | rewrite of a virus | rewritten version of a virus | modified virus ]

virus mutant [ mutation | dérivé | forme mutante d'un virus | version réécrite d'un virus | virus modifié ]
IT Security | Viral Diseases
Sécurité des TI | Maladies virales


A rare familial skeletal dysplasia with characteristics of multiple epiphyseal dysplasia with extremely retarded ossification. It has been described in 6 members of a unique consanguineous family. A mutation in PTHR1 gene is responsible for this synd

syndrome d'Eiken
SNOMEDCT-BE (disorder) / 720863002
SNOMEDCT-BE (disorder) / 720863002




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'de novo mutation'

Date index:2023-05-03 -

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