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Antenna diversity
Antenna diversity transponder
Diversity transponder
Non-directional antenna
Nondirectional antenna
Offer social services in diverse cultural communities
Omni antenna
Omni-antenna
Omnidirectional aerial
Omnidirectional antenna
Spaced aerial diversity
Spaced antenna diversity
Support cultural diversity
Support cultural multiplicity
Support diversity of cultures
Supporting cultural diversity
Triple spaced aerial diversity
Triple spaced antenna diversity

Traduction de «Antenna diversity » (Anglais → Français) :





spaced aerial diversity | spaced antenna diversity

diversité sur antennes espacées


triple spaced aerial diversity | triple spaced antenna diversity

diversité d'espace à trois antennes


diversity transponder [ antenna diversity transponder ]

transpondeur à diversité [ transpondeur à diversité d'antenne ]


Charcot-Marie-Tooth disease, type 4F (CMT4F) is a demyelinating CMT peripheral sensorimotor polyneuropathy. It is a rare form of CMT4 but the few reported families are from diverse ethnic groups: Lebanese Shiite Muslims, Hispanic North Americans, Nor

maladie de Charcot-Marie-Tooth type 4F


deliver social services in a diverse cultural community | provide social services in diverse cultural environments | deliver social services in diverse cultural communities | offer social services in diverse cultural communities

fournir des services sociaux au sein de différentes communautés culturelles


omnidirectional antenna [ nondirectional antenna | non-directional antenna | omnidirectional aerial | omni antenna | omni-antenna ]

antenne équidirective [ antenne sans effet directif | antenne omnidirectionnelle | antenne omnidirective ]


support diversity of cultures | supporting cultural diversity | support cultural diversity | support cultural multiplicity

favoriser la diversité culturelle


A newly described syndrome associated with a variable clinical phenotype including developmental delay, facial dysmorphism, short neck and diverse malformations. Eight cases have been reported to date. The most common facial features include eye anom

syndrome de microdélétion 6p22


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