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Anatomy of the auditory and vestibular system
Anatomy of the ear
Auditory anatomy
Cochlea
Cochlea of the ear
Hearing physiology
Human ear
Human ears
ITE hearing aid
In the ear hearing aid
In-the-ear hearing aid
Infundibulum of the cochlea
International Agency for the Promotion of Ear Care
Noise control at the ears of the listeners
Noise control at the receiver
Physiology of hearing
Physiology of the ear

Translation of "Cochlea the ear " (English → French) :

cochlea | cochlea of the ear

limaçon
IATE - Health
IATE - Health


hearing physiology | physiology of the ear | anatomy of the ear | physiology of hearing

physiologie de l’audition
knowledge
Savoir


A rare genetic multiple congenital anomalies syndrome with characteristics of second branchial arch anomalies (branchial cysts and fistulae), malformations of the outer, middle and inner ear associated with sensorineural, mixed or conductive hearing

syndrome branchio-otique
SNOMEDCT-BE (branchial cysts and fistulae), malformations of the outer, middle and inner ear associated with sensorineural, mixed or conductive hearing / 764810000
SNOMEDCT-BE (disorder) / 764810000


anatomy of the auditory and vestibular system | auditory anatomy | human ear | human ears

oreille humaine
knowledge
Savoir


in the ear hearing aid [ ITE hearing aid | in-the-ear hearing aid ]

prothèse intraconduit
Prostheses
Prothèses


noise control at the ears of the listeners | noise control at the receiver

contrôle du bruit à la réception
IATE - Health
IATE - Health


An extremely rare syndrome with characteristics of multiple unerupted permanent teeth, hypoplasia of the alveolar process and of the maxillo-zygomatic region, severe genu valgum and deformed ears. Consanguinity in the family suggested autosomal reces

syndrome de Stoelinga-de Koomen-Davis
SNOMEDCT-BE (disorder) / 723442008
SNOMEDCT-BE (disorder) / 723442008


infundibulum of the cochlea

extrémité infundibuliforme de la lame des contours
IATE - Health
IATE - Health


This syndrome has features of fibuloulnar dysostosis with renal anomalies. It has been described in two siblings born to nonconsanguinous parents. The syndrome is lethal at birth (respiratory failure). Clinical manifestations include ear and facial a

syndrome d'hypoplasie péroné-cubitus-anomalies rénales
SNOMEDCT-BE (respiratory failure). Clinical manifestations include ear and facial a / 716094008
SNOMEDCT-BE (disorder) / 716094008


International Agency for the Promotion of Ear Care

International Agency for the Promotion of Ear Care
International Bodies and Committees
Organismes et comités internationaux




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'Cochlea the ear'

Date index:2022-09-08 -

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