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Aarskog
Alfa-L-iduronidase deficiëntie
Cockayne
De Lange
Dubowitz
Holt-Oram
Hurler
Hurler-Scheie
Klippel-Trenaunay-Weber
Manisch depressief syndroom
Mucopolysaccharidose I
Mucopolysaccharidose I-S
Nagel-patella
Noonan
Prader-Willi
Robinow-Silverman-Smith
Rubinstein-Taybi
Russell-Silver
Scheie
Scheie syndroom
Seckel
Sirenomelie
Smith-Lemli-Opitz
Syndroom
Syndroom
Syndroom van
Syndroom van Abderhalden-Fanconi
Syndroom van Debré-Fanconi
Syndroom van Debré-de Toni-Fanconi
TAR-syndroom
Trombocytopenie met ontbreken van radius
VATER-syndroom
Ziektebeeld

Traduction de «scheie syndroom » (Néerlandais → Français) :

syndroom van | Hurler | syndroom van | Hurler-Scheie | syndroom van | Scheie

Syndrome de:Hurler | Hurler-Scheie | Scheie


alfa-L-iduronidase deficiëntie | mucopolysaccharidose I-S | Scheie syndroom

maladie de Scheie | mucopolysaccharidose de type I | mucopolysaccharidose de type I S | MPS I-S [Abbr.]


alfa-L-iduronidase deficiëntie | Hurler/Scheie syndroom | mucopolysaccharidose I

mucopolysaccharidose de type I | mucopolysaccharidose de type I H/S | syndrome de Hurler-Scheie | MPS I-H/S [Abbr.]






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 | 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: 2023-09-03
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