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Afford collateral security
Collateral chain
Collateral consanguinity
Collateral family
Collateral series
Consanguine
Consanguine marriage
Consanguineaous
Consanguineous
Consanguineous marriage
Furnish collateral security
Give collateral security
In-marriage
Intermarriage
Offer collateral security

Translation of "collateral consanguinity " (English → French) :

collateral consanguinity

consanguinité collatérale
IATE - LAW
IATE - LAW


collateral consanguinity

consanguinité collatérale
Law of Estates (common law) | PAJLO
Droit successoral (common law) | PAJLO


afford collateral security | furnish collateral security | give collateral security | offer collateral security

accorder une garantie | constituer une garantie | donner une garantie | fournir une garantie | offrir une garantie
IATE - FINANCE
IATE - FINANCE


This syndrome has characteristics of the association of total alopecia (present at birth), mild intellectual deficit and hypergonadotropic hypogonadism. It has been described in two brothers born to non consanguineous parents of Caucasian origin. Ele

syndrome d'alopécie-déficience intellectuelle-hypogonadisme hypergonadotrope
SNOMEDCT-BE (present at birth), mild intellectual deficit and hypergonadotropic hypogonadism. It has been described in two brothers born to non consanguineous parents of Caucasian origin. Ele / 720981000
SNOMEDCT-BE (disorder) / 720981000


consanguine marriage [ consanguineous marriage | intermarriage | in-marriage ]

mariage consanguin [ intermariage ]
Family Law (common law) | Demography | Sociology of Human Relations
Droit de la famille (common law) | Démographie | Sociologie des relations humaines


consanguineous [ consanguine | consanguineaous ]

consanguin
Social Organization | Anthropology
Organisation sociale | Anthropologie


consanguineous | consanguine

consanguin
ethnologie
ethnologie


collateral chain | collateral family | collateral series

chaîne collatérale | famille collatérale | série collatérale
IATE - Natural and applied sciences
IATE - Natural and applied sciences


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


Syndrome with the association of dentinogenesis imperfecta, delayed tooth eruption, facial dysmorphism, small stature, sensorineural hearing loss and mild intellectual deficit. It has been described in two brothers born to consanguineous parents. Tra

syndrome de dentinogenèse imparfaite-petite taille-surdité-déficience intellectuelle
SNOMEDCT-BE (disorder) / 721089006
SNOMEDCT-BE (disorder) / 721089006




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'collateral consanguinity'

Date index:2022-12-13 -

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