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Accessoire carpalia
Carpaal
Carpometacarpaal
Cleidocraniale dysostose
Congenitale pseudoartrose van clavicula
Distaal radio-ulnair gewricht
Humero-radio-ulnaire fusie
Humero-radio-ulnaire synostose
Intercarpaal
Macrodactylie
Misvorming van Madelung
Misvorming van Sprengel
Radio-ontvanger voor algemene doeleinden
Radio-renaal syndroom
Radio-ulnaire synostose
Radiocarpaal
Trifalangeale duim

Traduction de «required for radio » (Néerlandais → Français) :

TERMINOLOGIE
voir aussi les traductions en contexte ci-dessous












carpaal (bot) | carpometacarpaal (gewricht) | intercarpaal (gewricht) | metacarpaal (bot), proximaal uiteinde | radio-ulnair (gewricht), distaal | radiocarpaal (gewricht) | radius, distaal uiteinde | ulna, distaal uiteinde

Articulation:carpo-métacarpienne | cubito-radiale, distale | médio-carpienne | radio-carpienne | Cubitus, extrémité distale Métacarpiens, extrémité proximale Os du carpe Radius, extrémité distale


accessoire carpalia | cleidocraniale dysostose | congenitale pseudoartrose van clavicula | macrodactylie (vingers) | misvorming van Madelung | misvorming van Sprengel | radio-ulnaire synostose | trifalangeale duim

Carpocyphose [maladie de Madelung] Dysostose cléido-crânienne Macrodactylie (doigts) Malformation de Sprengel Os du carpe surnuméraire Pouce à trois phalanges Pseudarthrose congénitale de la clavicule Synostose radio-cubitale
TRADUCTIONS EN CONTEXTE
In order to regulate the quality and relevance of messages to the public, a prior licence is required for radio and TV information campaigns about human health and illness which refer directly or indirectly to medicines. This licence is normally issued by the Minister responsible following advice from the Commission for the supervision of advertising for medicines for human use.

In order to regulate the quality and relevance of messages to the public, a prior licence is required for radio and TV information campaigns about human health and illness which refer directly or indirectly to medicines. This licence is normally issued by the Minister responsible following advice from the Commission for the supervision of advertising for medicines for human use.


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