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Curtesy initiate
Estate by the curtesy initiate
Tenant by the curtesy initiate

Translation of "curtesy initiate " (English → French) :

curtesy initiate

bénéfice constitué du veuf
IATE - LAW
IATE - LAW


curtesy initiate

bénéfice constitué du veuf
IATE - Property Law (common law) | PAJLO
Droit des biens et de la propriété (common law) | PAJLO


tenant by the curtesy initiate

titulaire de bénéfice constitué du veuf
IATE - LAW
IATE - LAW


estate by the curtesy initiate

domaine viager constitué du veuf
IATE - LAW
IATE - LAW


estate by the curtesy initiate

domaine viager constitué du veuf
IATE - Property Law (common law) | PAJLO
Droit des biens et de la propriété (common law) | PAJLO


tenant by the curtesy initiate

titulaire du bénéfice constitué du veuf
IATE - Property Law (common law) | PAJLO
Droit des biens et de la propriété (common law) | PAJLO


Chancre of yaws Framboesia, initial or primary Initial framboesial ulcer Mother yaw

Chancre pianique Frambœsia initiale ou primaire Pian mère Ulcère frambœsial initial
WORLD HEALTH ORGANIZATION ICD-10: A66.0
WORLD HEALTH ORGANIZATION ICD-10: A66.0


A rare mitochondrial disease due to a defect in mitochondrial protein synthesis with a variable phenotype that includes onset in infancy or early childhood of failure to thrive and psychomotor regression (after initial normal development), as well as

déficit combiné de la phosphorylation oxydative type 7
SNOMEDCT-BE (after initial normal development), as well as / 763204003
SNOMEDCT-BE (disorder) / 763204003


A disorder of the skin and immune system with initial manifestation of a bumpy skin rash usually between the ages of 6 and 12 months, gradually spreading from the arms and legs to the torso and face. At about age 2, the rash fades leaving hyperpigmen

poïkilodermie avec neutropénie
SNOMEDCT-BE (disorder) / 772126000
SNOMEDCT-BE (disorder) / 772126000


A rare non-dystrophic myopathy with characteristics of slowly progressive muscular weakness and atrophy initially involving proximal lower limbs and hip girdle and later on shoulder girdle, proximal upper limbs and axial muscles. Ambulation is usuall

myopathie à corps d'inclusion héréditaire type 4
SNOMEDCT-BE (disorder) / 770786001
SNOMEDCT-BE (disorder) / 770786001




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'curtesy initiate'

Date index:2022-08-17 -

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