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Biological consanguinity
Consanguine
Consanguine marriage
Consanguineaous
Consanguineous
Consanguineous marriage
Consanguinity
Illegitimate descent
In-marriage
Intermarriage
Lineal consanguinity
Natural affiliation
Natural descent

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

TERMINOLOGY
see also In-Context Translations below
lineal consanguinity

consanguinité directe
Property Law (common law) | Law of Estates (common law) | PAJLO
Droit des biens et de la propriété (common law) | Droit successoral (common law) | PAJLO


lineal consanguinity

consanguinité directe
IATE - LAW
IATE - LAW


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


consanguineous [ consanguine | consanguineaous ]

consanguin
Social Organization | Anthropology
Organisation sociale | Anthropologie


consanguineous | consanguine

consanguin
ethnologie
ethnologie


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


biological consanguinity | illegitimate descent | natural affiliation | natural descent

filiation biologique | filiation naturelle
IATE - SOCIAL QUESTIONS
IATE - SOCIAL QUESTIONS




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
IN-CONTEXT TRANSLATIONS
(a) lineally by consanguinity or adoption;

a) en ligne directe, par consanguinité ou adoption;




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'lineal consanguinity'

Date index:2024-02-24 -

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