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Aarskog
Cockayne
Cooks-syndroom
De Lange
Dubowitz
Holt-Oram
Klippel-Trenaunay-Weber
Manisch depressief syndroom
Nagel-patella
Noonan
Prader-Willi
Robinow-Silverman-Smith
Rubinstein-Taybi
Russell-Silver
Seckel
Sirenomelie
Smith-Lemli-Opitz
Syndroom
Syndroom
Syndroom van
Syndroom van Abderhalden-Fanconi
Syndroom van Adams
Syndroom van Adams-Stokes
Syndroom van Bernard
Syndroom van Debré-Fanconi
Syndroom van Debré-de Toni-Fanconi
Syndroom van Horner
Syndroom van Horner-Bernard
Syndroom van Morgagni
TAR-syndroom
Trombocytopenie met ontbreken van radius
VATER-syndroom
Ziekte van Adams-Stokes
Ziektebeeld

Traduction de «cooks-syndroom » (Néerlandais → Français) :







syndroom van Adams | syndroom van Adams-Stokes | syndroom van Morgagni | ziekte van Adams-Stokes

syndrome d'Adams-Stokes


syndroom van Abderhalden-Fanconi | syndroom van Debré-de Toni-Fanconi | syndroom van Debré-Fanconi

diabète rénal gluco-phosphoaminé | syndrome de De Toni-Debré-Fanconi


syndroom van Bernard | syndroom van Horner | syndroom van Horner-Bernard

syndrome de Bernard | syndrome oculo-sympathique


syndroom van | Aarskog | syndroom van | Cockayne | syndroom van | de Lange | syndroom van | Dubowitz | syndroom van | Noonan | syndroom van | Prader-Willi | syndroom van | Robinow-Silverman-Smith | syndroom van | Russell-Silver | syndroom van | Seckel | syndroom van | Smith-Lemli-Opitz

Syndrome de:Aarskog | Cockayne | De Lange | Dubowitz | Noonan | Prader-Willi | Robinow-Silverman-Smith | Russell-Silver | Seckel | Smith-Lemli-Opitz


syndroom (van) | Holt-Oram | syndroom (van) | Klippel-Trenaunay-Weber | syndroom (van) | nagel-patella | syndroom (van) | Rubinstein-Taybi | syndroom (van) | sirenomelie | TAR-syndroom [trombocytopenie met ontbreken van radius] | VATER-syndroom

Ostéo-onychodysostose Syndrome de:Holt-Oram | Klippel-Trénaunay-Weber | onycho-arthro-ostéodysplasie | Rubinstein-Taybi | sirénomélie | thrombopénie avec absence de radius | VATER


SOLAMEN (segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus)-syndroom

syndrome d'hypertrophie segmentaire-lipomatose-malformation artérioveineuse-naevus épidermique


AHO-PHP (Albright hereditary osteodystrophy, pseudohypoparathyroidism)-syndroom Ia

pseudohypoparathyroïdie type 1A




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Date index: 2024-04-16
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