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Altimeter traverse
Altimeter traversing
Altimetric traverse
Altimetric traversing
Locomotive traverser
Main traverse
Non closed traverse
Open traverse
Open-end traverse
Opening traverse
Principal traverse
Pull-back traverse
Return traverse
Wagon traverser

Traduction de «Principal traverse » (Anglais → Français) :

main traverse | principal traverse

cheminement principal


altimetric traverse [ altimeter traverse | altimetric traversing | altimeter traversing ]

cheminement altimétrique


opening traverse | pull-back traverse | return traverse

traverse de rappel | traverse-entretoise


pull-back traverse [ opening traverse | return traverse ]

traverse de rappel [ traverse-entretoise ]


open traverse [ open-end traverse | non closed traverse ]

cheminement ouvert


A rare endocrine disease with characteristics of the triad of adult-onset diabetes mellitus, progressive hearing loss (usually presenting in the first decade of life and principally of low to moderate frequencies), and/or juvenile-onset optic atrophy

syndrome de Wolfram-like


Definition: The principal problem in men is erectile dysfunction (difficulty in developing or maintaining an erection suitable for satisfactory intercourse). In women, the principal problem is vaginal dryness or failure of lubrication. | Female sexual arousal disorder Male erectile disorder Psychogenic impotence

Définition: Le problème principal chez les hommes est un trouble des fonctions érectiles (difficulté à développer ou à maintenir une érection adéquate pour un rapport satisfaisant). Chez les femmes, le problème principal est une sécheresse vaginale ou un manque de lubrification. | Impuissance psychogène Trouble de:érection chez l'homme | réponse sexuelle chez la femme


locomotive traverser | wagon traverser

chariot-transbordeur | transbordeur


A potentially fatal neurological disease with characteristics of neuropathological lesions principally involving the brainstem, thalamus and putamen. It has been described in 11 members of one family. Onset occurs during early childhood, typically a

encéphalopathie nécrosante aigüe familiale


A rare chromosomal anomaly syndrome with highly variable phenotype. Principal characteristics are intrauterine growth retardation, failure to thrive, developmental delay, hypotonia, mild dysmorphic features (including microcephaly, short forehead, up

syndrome du chromosome 2 en anneau




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'Principal traverse' ->

Date index: 2023-07-20
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